Canonical Allele Identifier: CA500371183

Gene: MAPT

Linked Data

• MyVariant Identifiers: chr17:g.44091650C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46014284C>T , CM000679.2:g.46014284C>T	GRCh38
NC_000017.10:g.44091650C>T , CM000679.1:g.44091650C>T	GRCh37
NC_000017.9:g.41447487C>T	NCBI36
NG_007398.1:g.124864C>T
NG_007398.2:g.124822C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000420682.7:c.870C>T	ENSP00000413056.2:p.Thr290=
ENST00000703922.1:c.870C>T	ENSP00000515557.1:p.Thr290=
ENST00000703923.1:c.783C>T	ENSP00000515558.1:p.Thr261=
ENST00000703924.1:c.870C>T	ENSP00000515559.1:p.Thr290=
ENST00000703978.1:c.957C>T	ENSP00000515600.1:p.Thr319=
ENST00000703979.1:n.728C>T
ENST00000703980.1:n.183C>T
ENST00000703981.1:n.126C>T
ENST00000262410.10:c.2133C>T MANE Select	ENSP00000262410.6:p.Thr711=
ENST00000344290.10:c.1842C>T	ENSP00000340820.6:p.Thr614=
ENST00000351559.10:c.957C>T	ENSP00000303214.7:p.Thr319=
ENST00000535772.6:c.777C>T	ENSP00000443028.2:p.Thr259=
ENST00000680542.1:c.870C>T	ENSP00000505258.1:p.Thr290=
ENST00000680674.1:c.783C>T	ENSP00000505478.1:p.Thr261=
ENST00000262410.9:c.1908C>T	ENSP00000262410.5:p.Thr636=
ENST00000334239.12:c.690C>T	ENSP00000334886.8:p.Thr230=
ENST00000340799.9:c.870C>T	ENSP00000340438.5:p.Thr290=
ENST00000344290.9:c.1962C>T	ENSP00000340820.5:p.Thr654=
ENST00000351559.9:c.957C>T	ENSP00000303214.7:p.Thr319=
ENST00000415613.6:c.1962C>T	ENSP00000410838.2:p.Thr654=
ENST00000420682.6:c.870C>T	ENSP00000413056.2:p.Thr290=
ENST00000431008.7:c.864C>T	ENSP00000389250.3:p.Thr288=
ENST00000446361.7:c.783C>T	ENSP00000408975.3:p.Thr261=
ENST00000535772.5:c.864C>T	ENSP00000443028.1:p.Thr288=
ENST00000570299.5:n.777-4334C>T
ENST00000571987.5:c.1908C>T	ENSP00000458742.1:p.Thr636=
ENST00000574436.5:c.957C>T	ENSP00000460965.1:p.Thr319=
ENST00000576518.1:n.6149C>T
NM_001123066.3:c.1962C>T	NP_001116538.2:p.Thr654=
NM_001123067.3:c.870C>T	NP_001116539.1:p.Thr290=
NM_001203251.1:c.777C>T	NP_001190180.1:p.Thr259=
NM_001203252.1:c.864C>T	NP_001190181.1:p.Thr288=
NM_005910.5:c.957C>T	NP_005901.2:p.Thr319=
NM_016834.4:c.783C>T	NP_058518.1:p.Thr261=
NM_016835.4:c.1908C>T	NP_058519.3:p.Thr636=
NM_016841.4:c.690C>T	NP_058525.1:p.Thr230=
XM_005257362.3:c.2220C>T	XP_005257419.1:p.Thr740=
XM_005257364.3:c.2133C>T	XP_005257421.1:p.Thr711=
XM_005257365.3:c.2127C>T	XP_005257422.1:p.Thr709=
XM_005257366.2:c.2046C>T	XP_005257423.1:p.Thr682=
XM_005257367.3:c.2022C>T	XP_005257424.1:p.Thr674=
XM_005257368.3:c.1929C>T	XP_005257425.1:p.Thr643=
XM_005257369.3:c.1155C>T	XP_005257426.1:p.Thr385=
XM_005257370.3:c.1068C>T	XP_005257427.1:p.Thr356=
XM_005257371.3:c.981C>T	XP_005257428.1:p.Thr327=
XM_005257362.4:c.2220C>T	XP_005257419.1:p.Thr740=
XM_005257364.4:c.2133C>T	XP_005257421.1:p.Thr711=
XM_005257365.4:c.2127C>T	XP_005257422.1:p.Thr709=
XM_005257366.3:c.2046C>T	XP_005257423.1:p.Thr682=
XM_005257367.4:c.2022C>T	XP_005257424.1:p.Thr674=
XM_005257368.4:c.1929C>T	XP_005257425.1:p.Thr643=
XM_005257369.4:c.1155C>T	XP_005257426.1:p.Thr385=
XM_005257370.4:c.1068C>T	XP_005257427.1:p.Thr356=
XM_005257371.4:c.981C>T	XP_005257428.1:p.Thr327=
NM_001203251.2:c.777C>T	NP_001190180.1:p.Thr259=
NM_001377265.1:c.2133C>T MANE Select	NP_001364194.1:p.Thr711=
NM_001377266.1:c.1842C>T	NP_001364195.1:p.Thr614=
NM_001377267.1:c.771+6C>T	NP_001364196.1:n.771+6C>T
NM_001377268.1:c.690C>T	NP_001364197.1:p.Thr230=
NM_016834.5:c.783C>T	NP_058518.1:p.Thr261=
NM_016841.5:c.690C>T	NP_058525.1:p.Thr230=
NR_165166.1:n.788C>T
NM_001123066.4:c.1962C>T	NP_001116538.2:p.Thr654=
NM_001123067.4:c.870C>T	NP_001116539.1:p.Thr290=
NM_001203252.2:c.864C>T	NP_001190181.1:p.Thr288=
NM_005910.6:c.957C>T	NP_005901.2:p.Thr319=
NM_016835.5:c.1908C>T	NP_058519.3:p.Thr636=