Canonical Allele Identifier: CA1878829956

Gene: HSPA5

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.125238839A= , CM000671.2:g.125238839A=	GRCh38
NC_000009.11:g.128001118A= , CM000671.1:g.128001118A=	GRCh37
NC_000009.10:g.127040939A=	NCBI36
NG_027761.1:g.7549T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324460.7:c.997-12T= MANE Select	ENSP00000324173.6:n.997-12T=
ENST00000679355.1:n.1340T=
ENST00000679475.1:n.1581-12T=
ENST00000680032.1:c.997-12T=	ENSP00000506285.1:n.997-12T=
ENST00000680234.1:n.1253-12T=
ENST00000680257.1:n.1253-12T=
ENST00000680272.1:c.996+102T=	ENSP00000506097.1:n.996+102T=
ENST00000680494.1:n.2409T=
ENST00000680640.1:n.1948-12T=
ENST00000681045.1:n.1877-12T=
ENST00000681424.1:n.1340T=
ENST00000681540.1:n.1253-12T=
ENST00000681544.1:n.1328-12T=
ENST00000681675.1:n.1877-12T=
ENST00000681774.1:n.2219-12T=
ENST00000324460.6:c.997-12T=	ENSP00000324173.6:n.997-12T=
NM_005347.4:c.997-12T=	NP_005338.1:n.997-12T=
NM_005347.5:c.997-12T= MANE Select	NP_005338.1:n.997-12T=