Canonical Allele Identifier: CA1878829759

Gene: HSPA5

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.125238695C= , CM000671.2:g.125238695C=	GRCh38
NC_000009.11:g.128000974C= , CM000671.1:g.128000974C=	GRCh37
NC_000009.10:g.127040795C=	NCBI36
NG_027761.1:g.7693G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324460.7:c.1129G= MANE Select	ENSP00000324173.6:p.Glu377=
ENST00000679355.1:n.1484G=
ENST00000679475.1:n.1713G=
ENST00000680032.1:c.1129G=	ENSP00000506285.1:p.Glu377=
ENST00000680234.1:n.1385G=
ENST00000680257.1:n.1385G=
ENST00000680272.1:c.1015G=	ENSP00000506097.1:p.Glu339=
ENST00000680494.1:n.2553G=
ENST00000680640.1:n.2080G=
ENST00000681045.1:n.2009G=
ENST00000681424.1:n.1484G=
ENST00000681540.1:n.1385G=
ENST00000681544.1:n.1460G=
ENST00000681675.1:n.2009G=
ENST00000681774.1:n.2351G=
ENST00000324460.6:c.1129G=	ENSP00000324173.6:p.Glu377=
NM_005347.4:c.1129G=	NP_005338.1:p.Glu377=
NM_005347.5:c.1129G= MANE Select	NP_005338.1:p.Glu377=