Canonical Allele Identifier: CA1878829935

Gene: HSPA5

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.125238819G= , CM000671.2:g.125238819G=	GRCh38
NC_000009.11:g.128001098G= , CM000671.1:g.128001098G=	GRCh37
NC_000009.10:g.127040919G=	NCBI36
NG_027761.1:g.7569C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324460.7:c.1005C= MANE Select	ENSP00000324173.6:p.Phe335=
ENST00000679355.1:n.1360C=
ENST00000679475.1:n.1589C=
ENST00000680032.1:c.1005C=	ENSP00000506285.1:p.Phe335=
ENST00000680234.1:n.1261C=
ENST00000680257.1:n.1261C=
ENST00000680272.1:c.997-106C=	ENSP00000506097.1:n.997-106C=
ENST00000680494.1:n.2429C=
ENST00000680640.1:n.1956C=
ENST00000681045.1:n.1885C=
ENST00000681424.1:n.1360C=
ENST00000681540.1:n.1261C=
ENST00000681544.1:n.1336C=
ENST00000681675.1:n.1885C=
ENST00000681774.1:n.2227C=
ENST00000324460.6:c.1005C=	ENSP00000324173.6:p.Phe335=
NM_005347.4:c.1005C=	NP_005338.1:p.Phe335=
NM_005347.5:c.1005C= MANE Select	NP_005338.1:p.Phe335=