Canonical Allele Identifier: CA500644055

Gene: MAPT

Linked Data

• MyVariant Identifiers: chr17:g.44073991C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.45996625C>A , CM000679.2:g.45996625C>A	GRCh38
NC_000017.10:g.44073991C>A , CM000679.1:g.44073991C>A	GRCh37
NC_000017.9:g.41429828C>A	NCBI36
NG_007398.1:g.107205C>A
NG_007398.2:g.107163C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000420682.7:c.696C>A	ENSP00000413056.2:p.Gly232=
ENST00000703922.1:c.696C>A	ENSP00000515557.1:p.Gly232=
ENST00000703923.1:c.609C>A	ENSP00000515558.1:p.Gly203=
ENST00000703924.1:c.696C>A	ENSP00000515559.1:p.Gly232=
ENST00000703978.1:c.783C>A	ENSP00000515600.1:p.Gly261=
ENST00000703979.1:n.647C>A
ENST00000703980.1:n.15C>A
ENST00000262410.10:c.1959C>A MANE Select	ENSP00000262410.6:p.Gly653=
ENST00000344290.10:c.1761C>A	ENSP00000340820.6:p.Gly587=
ENST00000351559.10:c.783C>A	ENSP00000303214.7:p.Gly261=
ENST00000535772.6:c.696C>A	ENSP00000443028.2:p.Gly232=
ENST00000680542.1:c.696C>A	ENSP00000505258.1:p.Gly232=
ENST00000680674.1:c.609C>A	ENSP00000505478.1:p.Gly203=
ENST00000262410.9:c.1734C>A	ENSP00000262410.5:p.Gly578=
ENST00000334239.12:c.609C>A	ENSP00000334886.8:p.Gly203=
ENST00000340799.9:c.696C>A	ENSP00000340438.5:p.Gly232=
ENST00000344290.9:c.1788C>A	ENSP00000340820.5:p.Gly596=
ENST00000351559.9:c.783C>A	ENSP00000303214.7:p.Gly261=
ENST00000415613.6:c.1788C>A	ENSP00000410838.2:p.Gly596=
ENST00000420682.6:c.696C>A	ENSP00000413056.2:p.Gly232=
ENST00000431008.7:c.783C>A	ENSP00000389250.3:p.Gly261=
ENST00000446361.7:c.609C>A	ENSP00000408975.3:p.Gly203=
ENST00000535772.5:c.783C>A	ENSP00000443028.1:p.Gly261=
ENST00000570299.5:n.737C>A
ENST00000571987.5:c.1734C>A	ENSP00000458742.1:p.Gly578=
ENST00000574436.5:c.783C>A	ENSP00000460965.1:p.Gly261=
ENST00000576518.1:n.6068C>A
NM_001123066.3:c.1788C>A	NP_001116538.2:p.Gly596=
NM_001123067.3:c.696C>A	NP_001116539.1:p.Gly232=
NM_001203251.1:c.696C>A	NP_001190180.1:p.Gly232=
NM_001203252.1:c.783C>A	NP_001190181.1:p.Gly261=
NM_005910.5:c.783C>A	NP_005901.2:p.Gly261=
NM_016834.4:c.609C>A	NP_058518.1:p.Gly203=
NM_016835.4:c.1734C>A	NP_058519.3:p.Gly578=
NM_016841.4:c.609C>A	NP_058525.1:p.Gly203=
XM_005257362.3:c.2046C>A	XP_005257419.1:p.Gly682=
XM_005257364.3:c.1959C>A	XP_005257421.1:p.Gly653=
XM_005257365.3:c.2046C>A	XP_005257422.1:p.Gly682=
XM_005257366.2:c.1872C>A	XP_005257423.1:p.Gly624=
XM_005257367.3:c.1848C>A	XP_005257424.1:p.Gly616=
XM_005257368.3:c.1848C>A	XP_005257425.1:p.Gly616=
XM_005257369.3:c.981C>A	XP_005257426.1:p.Gly327=
XM_005257370.3:c.894C>A	XP_005257427.1:p.Gly298=
XM_005257371.3:c.807C>A	XP_005257428.1:p.Gly269=
XM_005257362.4:c.2046C>A	XP_005257419.1:p.Gly682=
XM_005257364.4:c.1959C>A	XP_005257421.1:p.Gly653=
XM_005257365.4:c.2046C>A	XP_005257422.1:p.Gly682=
XM_005257366.3:c.1872C>A	XP_005257423.1:p.Gly624=
XM_005257367.4:c.1848C>A	XP_005257424.1:p.Gly616=
XM_005257368.4:c.1848C>A	XP_005257425.1:p.Gly616=
XM_005257369.4:c.981C>A	XP_005257426.1:p.Gly327=
XM_005257370.4:c.894C>A	XP_005257427.1:p.Gly298=
XM_005257371.4:c.807C>A	XP_005257428.1:p.Gly269=
NM_001203251.2:c.696C>A	NP_001190180.1:p.Gly232=
NM_001377265.1:c.1959C>A MANE Select	NP_001364194.1:p.Gly653=
NM_001377266.1:c.1761C>A	NP_001364195.1:p.Gly587=
NM_001377267.1:c.696C>A	NP_001364196.1:p.Gly232=
NM_001377268.1:c.609C>A	NP_001364197.1:p.Gly203=
NM_016834.5:c.609C>A	NP_058518.1:p.Gly203=
NM_016841.5:c.609C>A	NP_058525.1:p.Gly203=
NR_165166.1:n.707C>A
NM_001123066.4:c.1788C>A	NP_001116538.2:p.Gly596=
NM_001123067.4:c.696C>A	NP_001116539.1:p.Gly232=
NM_001203252.2:c.783C>A	NP_001190181.1:p.Gly261=
NM_005910.6:c.783C>A	NP_005901.2:p.Gly261=
NM_016835.5:c.1734C>A	NP_058519.3:p.Gly578=