Canonical Allele Identifier: CA1878829945

Gene: HSPA5

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.125238826T= , CM000671.2:g.125238826T=	GRCh38
NC_000009.11:g.128001105T= , CM000671.1:g.128001105T=	GRCh37
NC_000009.10:g.127040926T=	NCBI36
NG_027761.1:g.7562A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324460.7:c.998A= MANE Select	ENSP00000324173.6:p.Asp333=
ENST00000679355.1:n.1353A=
ENST00000679475.1:n.1582A=
ENST00000680032.1:c.998A=	ENSP00000506285.1:p.Asp333=
ENST00000680234.1:n.1254A=
ENST00000680257.1:n.1254A=
ENST00000680272.1:c.997-113A=	ENSP00000506097.1:n.997-113A=
ENST00000680494.1:n.2422A=
ENST00000680640.1:n.1949A=
ENST00000681045.1:n.1878A=
ENST00000681424.1:n.1353A=
ENST00000681540.1:n.1254A=
ENST00000681544.1:n.1329A=
ENST00000681675.1:n.1878A=
ENST00000681774.1:n.2220A=
ENST00000324460.6:c.998A=	ENSP00000324173.6:p.Asp333=
NM_005347.4:c.998A=	NP_005338.1:p.Asp333=
NM_005347.5:c.998A= MANE Select	NP_005338.1:p.Asp333=