Canonical Allele Identifier: CA1878829727

Gene: HSPA5

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.125238664C= , CM000671.2:g.125238664C=	GRCh38
NC_000009.11:g.128000943C= , CM000671.1:g.128000943C=	GRCh37
NC_000009.10:g.127040764C=	NCBI36
NG_027761.1:g.7724G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324460.7:c.1160G= MANE Select	ENSP00000324173.6:p.Gly387=
ENST00000679355.1:n.1515G=
ENST00000679475.1:n.1744G=
ENST00000680032.1:c.1160G=	ENSP00000506285.1:p.Gly387=
ENST00000680234.1:n.1416G=
ENST00000680257.1:n.1416G=
ENST00000680272.1:c.1046G=	ENSP00000506097.1:p.Gly349=
ENST00000680494.1:n.2584G=
ENST00000680640.1:n.2111G=
ENST00000681045.1:n.2040G=
ENST00000681424.1:n.1515G=
ENST00000681540.1:n.1416G=
ENST00000681544.1:n.1491G=
ENST00000681675.1:n.2040G=
ENST00000681774.1:n.2382G=
ENST00000324460.6:c.1160G=	ENSP00000324173.6:p.Gly387=
NM_005347.4:c.1160G=	NP_005338.1:p.Gly387=
NM_005347.5:c.1160G= MANE Select	NP_005338.1:p.Gly387=