Canonical Allele Identifier: CA1878830039

Gene: HSPA5

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.125238900T= , CM000671.2:g.125238900T=	GRCh38
NC_000009.11:g.128001179T= , CM000671.1:g.128001179T=	GRCh37
NC_000009.10:g.127041000T=	NCBI36
NG_027761.1:g.7488A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324460.7:c.996+41A= MANE Select	ENSP00000324173.6:n.996+41A=
ENST00000679355.1:n.1279A=
ENST00000679475.1:n.1580+41A=
ENST00000680032.1:c.996+41A=	ENSP00000506285.1:n.996+41A=
ENST00000680234.1:n.1252+41A=
ENST00000680257.1:n.1252+41A=
ENST00000680272.1:c.996+41A=	ENSP00000506097.1:n.996+41A=
ENST00000680494.1:n.2348A=
ENST00000680640.1:n.1947+41A=
ENST00000681045.1:n.1876+41A=
ENST00000681424.1:n.1279A=
ENST00000681540.1:n.1252+41A=
ENST00000681544.1:n.1327+41A=
ENST00000681675.1:n.1876+41A=
ENST00000681774.1:n.2218+41A=
ENST00000324460.6:c.996+41A=	ENSP00000324173.6:n.996+41A=
NM_005347.4:c.996+41A=	NP_005338.1:n.996+41A=
NM_005347.5:c.996+41A= MANE Select	NP_005338.1:n.996+41A=