Canonical Allele Identifier: CA399984515

Gene: MAPT

Linked Data

• MyVariant Identifiers: chr17:g.44101442G>A (hg19) ; chr17:g.46024076G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46024076G>A , CM000679.2:g.46024076G>A	GRCh38
NC_000017.10:g.44101442G>A , CM000679.1:g.44101442G>A	GRCh37
NC_000017.9:g.41457287G>A	NCBI36
NG_007398.1:g.134664G>A
NG_007398.2:g.134614G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420682.7:c.1144G>A	ENSP00000413056.2:p.Val382Ile
ENST00000703922.1:c.1144G>A	ENSP00000515557.1:p.Val382Ile
ENST00000703923.1:c.1057G>A	ENSP00000515558.1:p.Val353Ile
ENST00000703924.1:c.1144G>A	ENSP00000515559.1:p.Val382Ile
ENST00000703978.1:c.1231G>A	ENSP00000515600.1:p.Val411Ile
ENST00000703980.1:n.457G>A
ENST00000703981.1:n.415G>A
ENST00000703982.1:n.649G>A
ENST00000262410.10:c.2407G>A MANE Select	ENSP00000262410.6:p.Val803Ile
ENST00000344290.10:c.2116G>A	ENSP00000340820.6:p.Val706Ile
ENST00000351559.10:c.1231G>A	ENSP00000303214.7:p.Val411Ile
ENST00000535772.6:c.1051G>A	ENSP00000443028.2:p.Val351Ile
ENST00000680542.1:c.1144G>A	ENSP00000505258.1:p.Val382Ile
ENST00000680674.1:c.1180G>A	ENSP00000505478.1:p.Val394Ile
ENST00000262410.9:c.2182G>A	ENSP00000262410.5:p.Val728Ile
ENST00000334239.12:c.964G>A	ENSP00000334886.8:p.Val322Ile
ENST00000340799.9:c.1144G>A	ENSP00000340438.5:p.Val382Ile
ENST00000344290.9:c.2236G>A	ENSP00000340820.5:p.Val746Ile
ENST00000351559.9:c.1231G>A	ENSP00000303214.7:p.Val411Ile
ENST00000415613.6:c.2236G>A	ENSP00000410838.2:p.Val746Ile
ENST00000420682.6:c.1144G>A	ENSP00000413056.2:p.Val382Ile
ENST00000431008.7:c.1138G>A	ENSP00000389250.3:p.Val380Ile
ENST00000446361.7:c.1057G>A	ENSP00000408975.3:p.Val353Ile
ENST00000535772.5:c.1138G>A	ENSP00000443028.1:p.Val380Ile
ENST00000571987.5:c.2182G>A	ENSP00000458742.1:p.Val728Ile
ENST00000574436.5:c.1231G>A	ENSP00000460965.1:p.Val411Ile
ENST00000576518.1:n.6423G>A
NM_001123066.3:c.2236G>A	NP_001116538.2:p.Val746Ile
NM_001123067.3:c.1144G>A	NP_001116539.1:p.Val382Ile
NM_001203251.1:c.1051G>A	NP_001190180.1:p.Val351Ile
NM_001203252.1:c.1138G>A	NP_001190181.1:p.Val380Ile
NM_005910.5:c.1231G>A	NP_005901.2:p.Val411Ile
NM_016834.4:c.1057G>A	NP_058518.1:p.Val353Ile
NM_016835.4:c.2182G>A	NP_058519.3:p.Val728Ile
NM_016841.4:c.964G>A	NP_058525.1:p.Val322Ile
XM_005257362.3:c.2494G>A	XP_005257419.1:p.Val832Ile
XM_005257364.3:c.2407G>A	XP_005257421.1:p.Val803Ile
XM_005257365.3:c.2401G>A	XP_005257422.1:p.Val801Ile
XM_005257366.2:c.2320G>A	XP_005257423.1:p.Val774Ile
XM_005257367.3:c.2296G>A	XP_005257424.1:p.Val766Ile
XM_005257368.3:c.2203G>A	XP_005257425.1:p.Val735Ile
XM_005257369.3:c.1429G>A	XP_005257426.1:p.Val477Ile
XM_005257370.3:c.1342G>A	XP_005257427.1:p.Val448Ile
XM_005257371.3:c.1255G>A	XP_005257428.1:p.Val419Ile
XM_005257362.4:c.2494G>A	XP_005257419.1:p.Val832Ile
XM_005257364.4:c.2407G>A	XP_005257421.1:p.Val803Ile
XM_005257365.4:c.2401G>A	XP_005257422.1:p.Val801Ile
XM_005257366.3:c.2320G>A	XP_005257423.1:p.Val774Ile
XM_005257367.4:c.2296G>A	XP_005257424.1:p.Val766Ile
XM_005257368.4:c.2203G>A	XP_005257425.1:p.Val735Ile
XM_005257369.4:c.1429G>A	XP_005257426.1:p.Val477Ile
XM_005257370.4:c.1342G>A	XP_005257427.1:p.Val448Ile
XM_005257371.4:c.1255G>A	XP_005257428.1:p.Val419Ile
NM_001203251.2:c.1051G>A	NP_001190180.1:p.Val351Ile
NM_001377265.1:c.2407G>A MANE Select	NP_001364194.1:p.Val803Ile
NM_001377266.1:c.2116G>A	NP_001364195.1:p.Val706Ile
NM_001377267.1:c.772-1041G>A	NP_001364196.1:n.772-1041G>A
NM_001377268.1:c.964G>A	NP_001364197.1:p.Val322Ile
NM_016834.5:c.1057G>A	NP_058518.1:p.Val353Ile
NM_016841.5:c.964G>A	NP_058525.1:p.Val322Ile
NR_165166.1:n.1062G>A
NM_001123066.4:c.2236G>A	NP_001116538.2:p.Val746Ile
NM_001123067.4:c.1144G>A	NP_001116539.1:p.Val382Ile
NM_001203252.2:c.1138G>A	NP_001190181.1:p.Val380Ile
NM_005910.6:c.1231G>A	NP_005901.2:p.Val411Ile
NM_016835.5:c.2182G>A	NP_058519.3:p.Val728Ile