Canonical Allele Identifier: CA399977960

Gene: MAPT

Linked Data

• MyVariant Identifiers: chr17:g.44073779T>A (hg19) ; chr17:g.45996413T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.45996413T>A , CM000679.2:g.45996413T>A	GRCh38
NC_000017.10:g.44073779T>A , CM000679.1:g.44073779T>A	GRCh37
NC_000017.9:g.41429616T>A	NCBI36
NG_007398.1:g.106993T>A
NG_007398.2:g.106951T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000420682.7:c.484T>A	ENSP00000413056.2:p.Ser162Thr
ENST00000703922.1:c.484T>A	ENSP00000515557.1:p.Ser162Thr
ENST00000703923.1:c.397T>A	ENSP00000515558.1:p.Ser133Thr
ENST00000703924.1:c.484T>A	ENSP00000515559.1:p.Ser162Thr
ENST00000703978.1:c.571T>A	ENSP00000515600.1:p.Ser191Thr
ENST00000703979.1:n.435T>A
ENST00000262410.10:c.1747T>A MANE Select	ENSP00000262410.6:p.Ser583Thr
ENST00000344290.10:c.1549T>A	ENSP00000340820.6:p.Ser517Thr
ENST00000351559.10:c.571T>A	ENSP00000303214.7:p.Ser191Thr
ENST00000535772.6:c.484T>A	ENSP00000443028.2:p.Ser162Thr
ENST00000680542.1:c.484T>A	ENSP00000505258.1:p.Ser162Thr
ENST00000680674.1:c.397T>A	ENSP00000505478.1:p.Ser133Thr
ENST00000262410.9:c.1522T>A	ENSP00000262410.5:p.Ser508Thr
ENST00000334239.12:c.397T>A	ENSP00000334886.8:p.Ser133Thr
ENST00000340799.9:c.484T>A	ENSP00000340438.5:p.Ser162Thr
ENST00000344290.9:c.1576T>A	ENSP00000340820.5:p.Ser526Thr
ENST00000351559.9:c.571T>A	ENSP00000303214.7:p.Ser191Thr
ENST00000415613.6:c.1576T>A	ENSP00000410838.2:p.Ser526Thr
ENST00000420682.6:c.484T>A	ENSP00000413056.2:p.Ser162Thr
ENST00000431008.7:c.571T>A	ENSP00000389250.3:p.Ser191Thr
ENST00000446361.7:c.397T>A	ENSP00000408975.3:p.Ser133Thr
ENST00000535772.5:c.571T>A	ENSP00000443028.1:p.Ser191Thr
ENST00000570299.5:n.525T>A
ENST00000571987.5:c.1522T>A	ENSP00000458742.1:p.Ser508Thr
ENST00000574436.5:c.571T>A	ENSP00000460965.1:p.Ser191Thr
ENST00000576518.1:n.5856T>A
NM_001123066.3:c.1576T>A	NP_001116538.2:p.Ser526Thr
NM_001123067.3:c.484T>A	NP_001116539.1:p.Ser162Thr
NM_001203251.1:c.484T>A	NP_001190180.1:p.Ser162Thr
NM_001203252.1:c.571T>A	NP_001190181.1:p.Ser191Thr
NM_005910.5:c.571T>A	NP_005901.2:p.Ser191Thr
NM_016834.4:c.397T>A	NP_058518.1:p.Ser133Thr
NM_016835.4:c.1522T>A	NP_058519.3:p.Ser508Thr
NM_016841.4:c.397T>A	NP_058525.1:p.Ser133Thr
XM_005257362.3:c.1834T>A	XP_005257419.1:p.Ser612Thr
XM_005257364.3:c.1747T>A	XP_005257421.1:p.Ser583Thr
XM_005257365.3:c.1834T>A	XP_005257422.1:p.Ser612Thr
XM_005257366.2:c.1660T>A	XP_005257423.1:p.Ser554Thr
XM_005257367.3:c.1636T>A	XP_005257424.1:p.Ser546Thr
XM_005257368.3:c.1636T>A	XP_005257425.1:p.Ser546Thr
XM_005257369.3:c.769T>A	XP_005257426.1:p.Ser257Thr
XM_005257370.3:c.682T>A	XP_005257427.1:p.Ser228Thr
XM_005257371.3:c.595T>A	XP_005257428.1:p.Ser199Thr
XM_005257362.4:c.1834T>A	XP_005257419.1:p.Ser612Thr
XM_005257364.4:c.1747T>A	XP_005257421.1:p.Ser583Thr
XM_005257365.4:c.1834T>A	XP_005257422.1:p.Ser612Thr
XM_005257366.3:c.1660T>A	XP_005257423.1:p.Ser554Thr
XM_005257367.4:c.1636T>A	XP_005257424.1:p.Ser546Thr
XM_005257368.4:c.1636T>A	XP_005257425.1:p.Ser546Thr
XM_005257369.4:c.769T>A	XP_005257426.1:p.Ser257Thr
XM_005257370.4:c.682T>A	XP_005257427.1:p.Ser228Thr
XM_005257371.4:c.595T>A	XP_005257428.1:p.Ser199Thr
NM_001203251.2:c.484T>A	NP_001190180.1:p.Ser162Thr
NM_001377265.1:c.1747T>A MANE Select	NP_001364194.1:p.Ser583Thr
NM_001377266.1:c.1549T>A	NP_001364195.1:p.Ser517Thr
NM_001377267.1:c.484T>A	NP_001364196.1:p.Ser162Thr
NM_001377268.1:c.397T>A	NP_001364197.1:p.Ser133Thr
NM_016834.5:c.397T>A	NP_058518.1:p.Ser133Thr
NM_016841.5:c.397T>A	NP_058525.1:p.Ser133Thr
NR_165166.1:n.591-96T>A
NM_001123066.4:c.1576T>A	NP_001116538.2:p.Ser526Thr
NM_001123067.4:c.484T>A	NP_001116539.1:p.Ser162Thr
NM_001203252.2:c.571T>A	NP_001190181.1:p.Ser191Thr
NM_005910.6:c.571T>A	NP_005901.2:p.Ser191Thr
NM_016835.5:c.1522T>A	NP_058519.3:p.Ser508Thr