Canonical Allele Identifier: CA399984289

Gene: MAPT

Linked Data

• MyVariant Identifiers: chr17:g.44101335A>T (hg19) ; chr17:g.46023969A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46023969A>T , CM000679.2:g.46023969A>T	GRCh38
NC_000017.10:g.44101335A>T , CM000679.1:g.44101335A>T	GRCh37
NC_000017.9:g.41457180A>T	NCBI36
NG_007398.1:g.134557A>T
NG_007398.2:g.134507A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000420682.7:c.1037A>T	ENSP00000413056.2:p.Lys346Met
ENST00000703922.1:c.1037A>T	ENSP00000515557.1:p.Lys346Met
ENST00000703923.1:c.950A>T	ENSP00000515558.1:p.Lys317Met
ENST00000703924.1:c.1037A>T	ENSP00000515559.1:p.Lys346Met
ENST00000703978.1:c.1124A>T	ENSP00000515600.1:p.Lys375Met
ENST00000703980.1:n.350A>T
ENST00000703981.1:n.308A>T
ENST00000703982.1:n.542A>T
ENST00000262410.10:c.2300A>T MANE Select	ENSP00000262410.6:p.Lys767Met
ENST00000344290.10:c.2009A>T	ENSP00000340820.6:p.Lys670Met
ENST00000351559.10:c.1124A>T	ENSP00000303214.7:p.Lys375Met
ENST00000535772.6:c.944A>T	ENSP00000443028.2:p.Lys315Met
ENST00000680542.1:c.1037A>T	ENSP00000505258.1:p.Lys346Met
ENST00000680674.1:c.1073A>T	ENSP00000505478.1:p.Lys358Met
ENST00000262410.9:c.2075A>T	ENSP00000262410.5:p.Lys692Met
ENST00000334239.12:c.857A>T	ENSP00000334886.8:p.Lys286Met
ENST00000340799.9:c.1037A>T	ENSP00000340438.5:p.Lys346Met
ENST00000344290.9:c.2129A>T	ENSP00000340820.5:p.Lys710Met
ENST00000351559.9:c.1124A>T	ENSP00000303214.7:p.Lys375Met
ENST00000415613.6:c.2129A>T	ENSP00000410838.2:p.Lys710Met
ENST00000420682.6:c.1037A>T	ENSP00000413056.2:p.Lys346Met
ENST00000431008.7:c.1031A>T	ENSP00000389250.3:p.Lys344Met
ENST00000446361.7:c.950A>T	ENSP00000408975.3:p.Lys317Met
ENST00000535772.5:c.1031A>T	ENSP00000443028.1:p.Lys344Met
ENST00000571987.5:c.2075A>T	ENSP00000458742.1:p.Lys692Met
ENST00000574436.5:c.1124A>T	ENSP00000460965.1:p.Lys375Met
ENST00000576518.1:n.6316A>T
NM_001123066.3:c.2129A>T	NP_001116538.2:p.Lys710Met
NM_001123067.3:c.1037A>T	NP_001116539.1:p.Lys346Met
NM_001203251.1:c.944A>T	NP_001190180.1:p.Lys315Met
NM_001203252.1:c.1031A>T	NP_001190181.1:p.Lys344Met
NM_005910.5:c.1124A>T	NP_005901.2:p.Lys375Met
NM_016834.4:c.950A>T	NP_058518.1:p.Lys317Met
NM_016835.4:c.2075A>T	NP_058519.3:p.Lys692Met
NM_016841.4:c.857A>T	NP_058525.1:p.Lys286Met
XM_005257362.3:c.2387A>T	XP_005257419.1:p.Lys796Met
XM_005257364.3:c.2300A>T	XP_005257421.1:p.Lys767Met
XM_005257365.3:c.2294A>T	XP_005257422.1:p.Lys765Met
XM_005257366.2:c.2213A>T	XP_005257423.1:p.Lys738Met
XM_005257367.3:c.2189A>T	XP_005257424.1:p.Lys730Met
XM_005257368.3:c.2096A>T	XP_005257425.1:p.Lys699Met
XM_005257369.3:c.1322A>T	XP_005257426.1:p.Lys441Met
XM_005257370.3:c.1235A>T	XP_005257427.1:p.Lys412Met
XM_005257371.3:c.1148A>T	XP_005257428.1:p.Lys383Met
XM_005257362.4:c.2387A>T	XP_005257419.1:p.Lys796Met
XM_005257364.4:c.2300A>T	XP_005257421.1:p.Lys767Met
XM_005257365.4:c.2294A>T	XP_005257422.1:p.Lys765Met
XM_005257366.3:c.2213A>T	XP_005257423.1:p.Lys738Met
XM_005257367.4:c.2189A>T	XP_005257424.1:p.Lys730Met
XM_005257368.4:c.2096A>T	XP_005257425.1:p.Lys699Met
XM_005257369.4:c.1322A>T	XP_005257426.1:p.Lys441Met
XM_005257370.4:c.1235A>T	XP_005257427.1:p.Lys412Met
XM_005257371.4:c.1148A>T	XP_005257428.1:p.Lys383Met
NM_001203251.2:c.944A>T	NP_001190180.1:p.Lys315Met
NM_001377265.1:c.2300A>T MANE Select	NP_001364194.1:p.Lys767Met
NM_001377266.1:c.2009A>T	NP_001364195.1:p.Lys670Met
NM_001377267.1:c.772-1148A>T	NP_001364196.1:n.772-1148A>T
NM_001377268.1:c.857A>T	NP_001364197.1:p.Lys286Met
NM_016834.5:c.950A>T	NP_058518.1:p.Lys317Met
NM_016841.5:c.857A>T	NP_058525.1:p.Lys286Met
NR_165166.1:n.955A>T
NM_001123066.4:c.2129A>T	NP_001116538.2:p.Lys710Met
NM_001123067.4:c.1037A>T	NP_001116539.1:p.Lys346Met
NM_001203252.2:c.1031A>T	NP_001190181.1:p.Lys344Met
NM_005910.6:c.1124A>T	NP_005901.2:p.Lys375Met
NM_016835.5:c.2075A>T	NP_058519.3:p.Lys692Met