Canonical Allele Identifier: CA500371160

Gene: MAPT

Linked Data

• MyVariant Identifiers: chr17:g.44091614A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46014248A>G , CM000679.2:g.46014248A>G	GRCh38
NC_000017.10:g.44091614A>G , CM000679.1:g.44091614A>G	GRCh37
NC_000017.9:g.41447451A>G	NCBI36
NG_007398.1:g.124828A>G
NG_007398.2:g.124786A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420682.7:c.834A>G	ENSP00000413056.2:p.Gln278=
ENST00000703922.1:c.834A>G	ENSP00000515557.1:p.Gln278=
ENST00000703923.1:c.747A>G	ENSP00000515558.1:p.Gln249=
ENST00000703924.1:c.834A>G	ENSP00000515559.1:p.Gln278=
ENST00000703978.1:c.921A>G	ENSP00000515600.1:p.Gln307=
ENST00000703979.1:n.692A>G
ENST00000703980.1:n.147A>G
ENST00000703981.1:n.90A>G
ENST00000262410.10:c.2097A>G MANE Select	ENSP00000262410.6:p.Gln699=
ENST00000344290.10:c.1806A>G	ENSP00000340820.6:p.Gln602=
ENST00000351559.10:c.921A>G	ENSP00000303214.7:p.Gln307=
ENST00000535772.6:c.741A>G	ENSP00000443028.2:p.Gln247=
ENST00000680542.1:c.834A>G	ENSP00000505258.1:p.Gln278=
ENST00000680674.1:c.747A>G	ENSP00000505478.1:p.Gln249=
ENST00000262410.9:c.1872A>G	ENSP00000262410.5:p.Gln624=
ENST00000334239.12:c.654A>G	ENSP00000334886.8:p.Gln218=
ENST00000340799.9:c.834A>G	ENSP00000340438.5:p.Gln278=
ENST00000344290.9:c.1926A>G	ENSP00000340820.5:p.Gln642=
ENST00000351559.9:c.921A>G	ENSP00000303214.7:p.Gln307=
ENST00000415613.6:c.1926A>G	ENSP00000410838.2:p.Gln642=
ENST00000420682.6:c.834A>G	ENSP00000413056.2:p.Gln278=
ENST00000431008.7:c.828A>G	ENSP00000389250.3:p.Gln276=
ENST00000446361.7:c.747A>G	ENSP00000408975.3:p.Gln249=
ENST00000535772.5:c.828A>G	ENSP00000443028.1:p.Gln276=
ENST00000570299.5:n.777-4370A>G
ENST00000571987.5:c.1872A>G	ENSP00000458742.1:p.Gln624=
ENST00000574436.5:c.921A>G	ENSP00000460965.1:p.Gln307=
ENST00000576518.1:n.6113A>G
NM_001123066.3:c.1926A>G	NP_001116538.2:p.Gln642=
NM_001123067.3:c.834A>G	NP_001116539.1:p.Gln278=
NM_001203251.1:c.741A>G	NP_001190180.1:p.Gln247=
NM_001203252.1:c.828A>G	NP_001190181.1:p.Gln276=
NM_005910.5:c.921A>G	NP_005901.2:p.Gln307=
NM_016834.4:c.747A>G	NP_058518.1:p.Gln249=
NM_016835.4:c.1872A>G	NP_058519.3:p.Gln624=
NM_016841.4:c.654A>G	NP_058525.1:p.Gln218=
XM_005257362.3:c.2184A>G	XP_005257419.1:p.Gln728=
XM_005257364.3:c.2097A>G	XP_005257421.1:p.Gln699=
XM_005257365.3:c.2091A>G	XP_005257422.1:p.Gln697=
XM_005257366.2:c.2010A>G	XP_005257423.1:p.Gln670=
XM_005257367.3:c.1986A>G	XP_005257424.1:p.Gln662=
XM_005257368.3:c.1893A>G	XP_005257425.1:p.Gln631=
XM_005257369.3:c.1119A>G	XP_005257426.1:p.Gln373=
XM_005257370.3:c.1032A>G	XP_005257427.1:p.Gln344=
XM_005257371.3:c.945A>G	XP_005257428.1:p.Gln315=
XM_005257362.4:c.2184A>G	XP_005257419.1:p.Gln728=
XM_005257364.4:c.2097A>G	XP_005257421.1:p.Gln699=
XM_005257365.4:c.2091A>G	XP_005257422.1:p.Gln697=
XM_005257366.3:c.2010A>G	XP_005257423.1:p.Gln670=
XM_005257367.4:c.1986A>G	XP_005257424.1:p.Gln662=
XM_005257368.4:c.1893A>G	XP_005257425.1:p.Gln631=
XM_005257369.4:c.1119A>G	XP_005257426.1:p.Gln373=
XM_005257370.4:c.1032A>G	XP_005257427.1:p.Gln344=
XM_005257371.4:c.945A>G	XP_005257428.1:p.Gln315=
NM_001203251.2:c.741A>G	NP_001190180.1:p.Gln247=
NM_001377265.1:c.2097A>G MANE Select	NP_001364194.1:p.Gln699=
NM_001377266.1:c.1806A>G	NP_001364195.1:p.Gln602=
NM_001377267.1:c.741A>G	NP_001364196.1:p.Gln247=
NM_001377268.1:c.654A>G	NP_001364197.1:p.Gln218=
NM_016834.5:c.747A>G	NP_058518.1:p.Gln249=
NM_016841.5:c.654A>G	NP_058525.1:p.Gln218=
NR_165166.1:n.752A>G
NM_001123066.4:c.1926A>G	NP_001116538.2:p.Gln642=
NM_001123067.4:c.834A>G	NP_001116539.1:p.Gln278=
NM_001203252.2:c.828A>G	NP_001190181.1:p.Gln276=
NM_005910.6:c.921A>G	NP_005901.2:p.Gln307=
NM_016835.5:c.1872A>G	NP_058519.3:p.Gln624=