Canonical Allele Identifier: CA399983651

Gene: MAPT

Linked Data

• MyVariant Identifiers: chr17:g.44096001G>T (hg19) ; chr17:g.46018635G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46018635G>T , CM000679.2:g.46018635G>T	GRCh38
NC_000017.10:g.44096001G>T , CM000679.1:g.44096001G>T	GRCh37
NC_000017.9:g.41451848G>T	NCBI36
NG_007398.1:g.129225G>T
NG_007398.2:g.129173G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000420682.7:c.928G>T	ENSP00000413056.2:p.Val310Leu
ENST00000703922.1:c.928G>T	ENSP00000515557.1:p.Val310Leu
ENST00000703923.1:c.841G>T	ENSP00000515558.1:p.Val281Leu
ENST00000703924.1:c.928G>T	ENSP00000515559.1:p.Val310Leu
ENST00000703978.1:c.1015G>T	ENSP00000515600.1:p.Val339Leu
ENST00000703979.1:n.786G>T
ENST00000703980.1:n.241G>T
ENST00000703981.1:n.199G>T
ENST00000703982.1:n.433G>T
ENST00000262410.10:c.2191G>T MANE Select	ENSP00000262410.6:p.Val731Leu
ENST00000344290.10:c.1900G>T	ENSP00000340820.6:p.Val634Leu
ENST00000351559.10:c.1015G>T	ENSP00000303214.7:p.Val339Leu
ENST00000535772.6:c.835G>T	ENSP00000443028.2:p.Val279Leu
ENST00000680542.1:c.928G>T	ENSP00000505258.1:p.Val310Leu
ENST00000680674.1:c.964G>T	ENSP00000505478.1:p.Val322Leu
ENST00000262410.9:c.1966G>T	ENSP00000262410.5:p.Val656Leu
ENST00000334239.12:c.748G>T	ENSP00000334886.8:p.Val250Leu
ENST00000340799.9:c.928G>T	ENSP00000340438.5:p.Val310Leu
ENST00000344290.9:c.2020G>T	ENSP00000340820.5:p.Val674Leu
ENST00000351559.9:c.1015G>T	ENSP00000303214.7:p.Val339Leu
ENST00000415613.6:c.2020G>T	ENSP00000410838.2:p.Val674Leu
ENST00000420682.6:c.928G>T	ENSP00000413056.2:p.Val310Leu
ENST00000431008.7:c.922G>T	ENSP00000389250.3:p.Val308Leu
ENST00000446361.7:c.841G>T	ENSP00000408975.3:p.Val281Leu
ENST00000535772.5:c.922G>T	ENSP00000443028.1:p.Val308Leu
ENST00000570299.5:n.794G>T
ENST00000571987.5:c.1966G>T	ENSP00000458742.1:p.Val656Leu
ENST00000574436.5:c.1015G>T	ENSP00000460965.1:p.Val339Leu
ENST00000576518.1:n.6207G>T
NM_001123066.3:c.2020G>T	NP_001116538.2:p.Val674Leu
NM_001123067.3:c.928G>T	NP_001116539.1:p.Val310Leu
NM_001203251.1:c.835G>T	NP_001190180.1:p.Val279Leu
NM_001203252.1:c.922G>T	NP_001190181.1:p.Val308Leu
NM_005910.5:c.1015G>T	NP_005901.2:p.Val339Leu
NM_016834.4:c.841G>T	NP_058518.1:p.Val281Leu
NM_016835.4:c.1966G>T	NP_058519.3:p.Val656Leu
NM_016841.4:c.748G>T	NP_058525.1:p.Val250Leu
XM_005257362.3:c.2278G>T	XP_005257419.1:p.Val760Leu
XM_005257364.3:c.2191G>T	XP_005257421.1:p.Val731Leu
XM_005257365.3:c.2185G>T	XP_005257422.1:p.Val729Leu
XM_005257366.2:c.2104G>T	XP_005257423.1:p.Val702Leu
XM_005257367.3:c.2080G>T	XP_005257424.1:p.Val694Leu
XM_005257368.3:c.1987G>T	XP_005257425.1:p.Val663Leu
XM_005257369.3:c.1213G>T	XP_005257426.1:p.Val405Leu
XM_005257370.3:c.1126G>T	XP_005257427.1:p.Val376Leu
XM_005257371.3:c.1039G>T	XP_005257428.1:p.Val347Leu
XM_005257362.4:c.2278G>T	XP_005257419.1:p.Val760Leu
XM_005257364.4:c.2191G>T	XP_005257421.1:p.Val731Leu
XM_005257365.4:c.2185G>T	XP_005257422.1:p.Val729Leu
XM_005257366.3:c.2104G>T	XP_005257423.1:p.Val702Leu
XM_005257367.4:c.2080G>T	XP_005257424.1:p.Val694Leu
XM_005257368.4:c.1987G>T	XP_005257425.1:p.Val663Leu
XM_005257369.4:c.1213G>T	XP_005257426.1:p.Val405Leu
XM_005257370.4:c.1126G>T	XP_005257427.1:p.Val376Leu
XM_005257371.4:c.1039G>T	XP_005257428.1:p.Val347Leu
NM_001203251.2:c.835G>T	NP_001190180.1:p.Val279Leu
NM_001377265.1:c.2191G>T MANE Select	NP_001364194.1:p.Val731Leu
NM_001377266.1:c.1900G>T	NP_001364195.1:p.Val634Leu
NM_001377267.1:c.771+4357G>T	NP_001364196.1:n.771+4357G>T
NM_001377268.1:c.748G>T	NP_001364197.1:p.Val250Leu
NM_016834.5:c.841G>T	NP_058518.1:p.Val281Leu
NM_016841.5:c.748G>T	NP_058525.1:p.Val250Leu
NR_165166.1:n.846G>T
NM_001123066.4:c.2020G>T	NP_001116538.2:p.Val674Leu
NM_001123067.4:c.928G>T	NP_001116539.1:p.Val310Leu
NM_001203252.2:c.922G>T	NP_001190181.1:p.Val308Leu
NM_005910.6:c.1015G>T	NP_005901.2:p.Val339Leu
NM_016835.5:c.1966G>T	NP_058519.3:p.Val656Leu