Canonical Allele Identifier: CA2638361154

Gene: MAPT

Linked Data

• gnomAD v4: 17-45979003-C-CAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.45979013_45979015dup , CM000679.2:g.45979013_45979015dup	GRCh38
NC_000017.10:g.44056379_44056381dup , CM000679.1:g.44056379_44056381dup	GRCh37
NC_000017.9:g.41412215_41412217dup	NCBI36
NG_007398.1:g.89592_89594dup
NG_007398.2:g.89551_89553dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000420682.7:c.286+573_286+575dup	ENSP00000413056.2:n.286+573_286+575dup
ENST00000703922.1:c.286+573_286+575dup	ENSP00000515557.1:n.286+573_286+575dup
ENST00000703923.1:c.199+573_199+575dup	ENSP00000515558.1:n.199+573_199+575dup
ENST00000703924.1:c.286+573_286+575dup	ENSP00000515559.1:n.286+573_286+575dup
ENST00000703975.1:n.330+573_330+575dup
ENST00000703976.1:n.398+573_398+575dup
ENST00000703977.1:n.240+573_240+575dup
ENST00000703978.1:c.373+573_373+575dup	ENSP00000515600.1:n.373+573_373+575dup
ENST00000703979.1:n.237+7068_237+7070dup
ENST00000262410.10:c.286+573_286+575dup MANE Select	ENSP00000262410.6:n.286+573_286+575dup
ENST00000344290.10:c.286+573_286+575dup	ENSP00000340820.6:n.286+573_286+575dup
ENST00000351559.10:c.373+573_373+575dup	ENSP00000303214.7:n.373+573_373+575dup
ENST00000535772.6:c.286+573_286+575dup	ENSP00000443028.2:n.286+573_286+575dup
ENST00000680542.1:c.286+573_286+575dup	ENSP00000505258.1:n.286+573_286+575dup
ENST00000680674.1:c.199+573_199+575dup	ENSP00000505478.1:n.199+573_199+575dup
ENST00000262410.9:c.373+573_373+575dup	ENSP00000262410.5:n.373+573_373+575dup
ENST00000334239.12:c.199+573_199+575dup	ENSP00000334886.8:n.199+573_199+575dup
ENST00000340799.9:c.286+573_286+575dup	ENSP00000340438.5:n.286+573_286+575dup
ENST00000344290.9:c.373+573_373+575dup	ENSP00000340820.5:n.373+573_373+575dup
ENST00000351559.9:c.373+573_373+575dup	ENSP00000303214.7:n.373+573_373+575dup
ENST00000415613.6:c.373+573_373+575dup	ENSP00000410838.2:n.373+573_373+575dup
ENST00000420682.6:c.286+573_286+575dup	ENSP00000413056.2:n.286+573_286+575dup
ENST00000431008.7:c.373+573_373+575dup	ENSP00000389250.3:n.373+573_373+575dup
ENST00000446361.7:c.199+573_199+575dup	ENSP00000408975.3:n.199+573_199+575dup
ENST00000535772.5:c.373+573_373+575dup	ENSP00000443028.1:n.373+573_373+575dup
ENST00000570299.5:n.327+573_327+575dup
ENST00000571987.5:c.373+573_373+575dup	ENSP00000458742.1:n.373+573_373+575dup
ENST00000572440.1:n.3522_3524dup
ENST00000574436.5:c.373+573_373+575dup	ENSP00000460965.1:n.373+573_373+575dup
ENST00000576518.1:n.5658+573_5658+575dup
NM_001123066.3:c.373+573_373+575dup	NP_001116538.2:n.373+573_373+575dup
NM_001123067.3:c.286+573_286+575dup	NP_001116539.1:n.286+573_286+575dup
NM_001203251.1:c.286+573_286+575dup	NP_001190180.1:n.286+573_286+575dup
NM_001203252.1:c.373+573_373+575dup	NP_001190181.1:n.373+573_373+575dup
NM_005910.5:c.373+573_373+575dup	NP_005901.2:n.373+573_373+575dup
NM_016834.4:c.199+573_199+575dup	NP_058518.1:n.199+573_199+575dup
NM_016835.4:c.373+573_373+575dup	NP_058519.3:n.373+573_373+575dup
NM_016841.4:c.199+573_199+575dup	NP_058525.1:n.199+573_199+575dup
XM_005257362.3:c.373+573_373+575dup	XP_005257419.1:n.373+573_373+575dup
XM_005257364.3:c.286+573_286+575dup	XP_005257421.1:n.286+573_286+575dup
XM_005257365.3:c.373+573_373+575dup	XP_005257422.1:n.373+573_373+575dup
XM_005257366.2:c.199+573_199+575dup	XP_005257423.1:n.199+573_199+575dup
XM_005257367.3:c.373+573_373+575dup	XP_005257424.1:n.373+573_373+575dup
XM_005257368.3:c.373+573_373+575dup	XP_005257425.1:n.373+573_373+575dup
XM_005257369.3:c.373+573_373+575dup	XP_005257426.1:n.373+573_373+575dup
XM_005257370.3:c.286+573_286+575dup	XP_005257427.1:n.286+573_286+575dup
XM_005257371.3:c.199+573_199+575dup	XP_005257428.1:n.199+573_199+575dup
XM_005257362.4:c.373+573_373+575dup	XP_005257419.1:n.373+573_373+575dup
XM_005257364.4:c.286+573_286+575dup	XP_005257421.1:n.286+573_286+575dup
XM_005257365.4:c.373+573_373+575dup	XP_005257422.1:n.373+573_373+575dup
XM_005257366.3:c.199+573_199+575dup	XP_005257423.1:n.199+573_199+575dup
XM_005257367.4:c.373+573_373+575dup	XP_005257424.1:n.373+573_373+575dup
XM_005257368.4:c.373+573_373+575dup	XP_005257425.1:n.373+573_373+575dup
XM_005257369.4:c.373+573_373+575dup	XP_005257426.1:n.373+573_373+575dup
XM_005257370.4:c.286+573_286+575dup	XP_005257427.1:n.286+573_286+575dup
XM_005257371.4:c.199+573_199+575dup	XP_005257428.1:n.199+573_199+575dup
NM_001203251.2:c.286+573_286+575dup	NP_001190180.1:n.286+573_286+575dup
NM_001377265.1:c.286+573_286+575dup MANE Select	NP_001364194.1:n.286+573_286+575dup
NM_001377266.1:c.286+573_286+575dup	NP_001364195.1:n.286+573_286+575dup
NM_001377267.1:c.286+573_286+575dup	NP_001364196.1:n.286+573_286+575dup
NM_001377268.1:c.199+573_199+575dup	NP_001364197.1:n.199+573_199+575dup
NM_016834.5:c.199+573_199+575dup	NP_058518.1:n.199+573_199+575dup
NM_016841.5:c.199+573_199+575dup	NP_058525.1:n.199+573_199+575dup
NR_165166.1:n.436+573_436+575dup
NM_001123066.4:c.373+573_373+575dup	NP_001116538.2:n.373+573_373+575dup
NM_001123067.4:c.286+573_286+575dup	NP_001116539.1:n.286+573_286+575dup
NM_001203252.2:c.373+573_373+575dup	NP_001190181.1:n.373+573_373+575dup
NM_005910.6:c.373+573_373+575dup	NP_005901.2:n.373+573_373+575dup
NM_016835.5:c.373+573_373+575dup	NP_058519.3:n.373+573_373+575dup