Canonical Allele Identifier: CA399983658

Gene: MAPT

Linked Data

• gnomAD v4: 17-46018639-A-C
• MyVariant Identifiers: chr17:g.44096005A>C (hg19) ; chr17:g.46018639A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46018639A>C , CM000679.2:g.46018639A>C	GRCh38
NC_000017.10:g.44096005A>C , CM000679.1:g.44096005A>C	GRCh37
NC_000017.9:g.41451852A>C	NCBI36
NG_007398.1:g.129229A>C
NG_007398.2:g.129177A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000420682.7:c.932A>C	ENSP00000413056.2:p.Lys311Thr
ENST00000703922.1:c.932A>C	ENSP00000515557.1:p.Lys311Thr
ENST00000703923.1:c.845A>C	ENSP00000515558.1:p.Lys282Thr
ENST00000703924.1:c.932A>C	ENSP00000515559.1:p.Lys311Thr
ENST00000703978.1:c.1019A>C	ENSP00000515600.1:p.Lys340Thr
ENST00000703979.1:n.790A>C
ENST00000703980.1:n.245A>C
ENST00000703981.1:n.203A>C
ENST00000703982.1:n.437A>C
ENST00000262410.10:c.2195A>C MANE Select	ENSP00000262410.6:p.Lys732Thr
ENST00000344290.10:c.1904A>C	ENSP00000340820.6:p.Lys635Thr
ENST00000351559.10:c.1019A>C	ENSP00000303214.7:p.Lys340Thr
ENST00000535772.6:c.839A>C	ENSP00000443028.2:p.Lys280Thr
ENST00000680542.1:c.932A>C	ENSP00000505258.1:p.Lys311Thr
ENST00000680674.1:c.968A>C	ENSP00000505478.1:p.Lys323Thr
ENST00000262410.9:c.1970A>C	ENSP00000262410.5:p.Lys657Thr
ENST00000334239.12:c.752A>C	ENSP00000334886.8:p.Lys251Thr
ENST00000340799.9:c.932A>C	ENSP00000340438.5:p.Lys311Thr
ENST00000344290.9:c.2024A>C	ENSP00000340820.5:p.Lys675Thr
ENST00000351559.9:c.1019A>C	ENSP00000303214.7:p.Lys340Thr
ENST00000415613.6:c.2024A>C	ENSP00000410838.2:p.Lys675Thr
ENST00000420682.6:c.932A>C	ENSP00000413056.2:p.Lys311Thr
ENST00000431008.7:c.926A>C	ENSP00000389250.3:p.Lys309Thr
ENST00000446361.7:c.845A>C	ENSP00000408975.3:p.Lys282Thr
ENST00000535772.5:c.926A>C	ENSP00000443028.1:p.Lys309Thr
ENST00000570299.5:n.798A>C
ENST00000571987.5:c.1970A>C	ENSP00000458742.1:p.Lys657Thr
ENST00000574436.5:c.1019A>C	ENSP00000460965.1:p.Lys340Thr
ENST00000576518.1:n.6211A>C
NM_001123066.3:c.2024A>C	NP_001116538.2:p.Lys675Thr
NM_001123067.3:c.932A>C	NP_001116539.1:p.Lys311Thr
NM_001203251.1:c.839A>C	NP_001190180.1:p.Lys280Thr
NM_001203252.1:c.926A>C	NP_001190181.1:p.Lys309Thr
NM_005910.5:c.1019A>C	NP_005901.2:p.Lys340Thr
NM_016834.4:c.845A>C	NP_058518.1:p.Lys282Thr
NM_016835.4:c.1970A>C	NP_058519.3:p.Lys657Thr
NM_016841.4:c.752A>C	NP_058525.1:p.Lys251Thr
XM_005257362.3:c.2282A>C	XP_005257419.1:p.Lys761Thr
XM_005257364.3:c.2195A>C	XP_005257421.1:p.Lys732Thr
XM_005257365.3:c.2189A>C	XP_005257422.1:p.Lys730Thr
XM_005257366.2:c.2108A>C	XP_005257423.1:p.Lys703Thr
XM_005257367.3:c.2084A>C	XP_005257424.1:p.Lys695Thr
XM_005257368.3:c.1991A>C	XP_005257425.1:p.Lys664Thr
XM_005257369.3:c.1217A>C	XP_005257426.1:p.Lys406Thr
XM_005257370.3:c.1130A>C	XP_005257427.1:p.Lys377Thr
XM_005257371.3:c.1043A>C	XP_005257428.1:p.Lys348Thr
XM_005257362.4:c.2282A>C	XP_005257419.1:p.Lys761Thr
XM_005257364.4:c.2195A>C	XP_005257421.1:p.Lys732Thr
XM_005257365.4:c.2189A>C	XP_005257422.1:p.Lys730Thr
XM_005257366.3:c.2108A>C	XP_005257423.1:p.Lys703Thr
XM_005257367.4:c.2084A>C	XP_005257424.1:p.Lys695Thr
XM_005257368.4:c.1991A>C	XP_005257425.1:p.Lys664Thr
XM_005257369.4:c.1217A>C	XP_005257426.1:p.Lys406Thr
XM_005257370.4:c.1130A>C	XP_005257427.1:p.Lys377Thr
XM_005257371.4:c.1043A>C	XP_005257428.1:p.Lys348Thr
NM_001203251.2:c.839A>C	NP_001190180.1:p.Lys280Thr
NM_001377265.1:c.2195A>C MANE Select	NP_001364194.1:p.Lys732Thr
NM_001377266.1:c.1904A>C	NP_001364195.1:p.Lys635Thr
NM_001377267.1:c.771+4361A>C	NP_001364196.1:n.771+4361A>C
NM_001377268.1:c.752A>C	NP_001364197.1:p.Lys251Thr
NM_016834.5:c.845A>C	NP_058518.1:p.Lys282Thr
NM_016841.5:c.752A>C	NP_058525.1:p.Lys251Thr
NR_165166.1:n.850A>C
NM_001123066.4:c.2024A>C	NP_001116538.2:p.Lys675Thr
NM_001123067.4:c.932A>C	NP_001116539.1:p.Lys311Thr
NM_001203252.2:c.926A>C	NP_001190181.1:p.Lys309Thr
NM_005910.6:c.1019A>C	NP_005901.2:p.Lys340Thr
NM_016835.5:c.1970A>C	NP_058519.3:p.Lys657Thr