Canonical Allele Identifier: CA467209645

Gene: HSPA5

Linked Data

• MyVariant Identifiers: chr9:g.128001235A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.125238956A>G , CM000671.2:g.125238956A>G	GRCh38
NC_000009.11:g.128001235A>G , CM000671.1:g.128001235A>G	GRCh37
NC_000009.10:g.127041056A>G	NCBI36
NG_027761.1:g.7432T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324460.7:c.981T>C MANE Select	ENSP00000324173.6:p.Phe327=
ENST00000679355.1:n.1223T>C
ENST00000679475.1:n.1565T>C
ENST00000680032.1:c.981T>C	ENSP00000506285.1:p.Phe327=
ENST00000680234.1:n.1237T>C
ENST00000680257.1:n.1237T>C
ENST00000680272.1:c.981T>C	ENSP00000506097.1:p.Phe327=
ENST00000680494.1:n.2292T>C
ENST00000680640.1:n.1932T>C
ENST00000681045.1:n.1861T>C
ENST00000681424.1:n.1223T>C
ENST00000681540.1:n.1237T>C
ENST00000681544.1:n.1312T>C
ENST00000681675.1:n.1861T>C
ENST00000681774.1:n.2203T>C
ENST00000324460.6:c.981T>C	ENSP00000324173.6:p.Phe327=
NM_005347.4:c.981T>C	NP_005338.1:p.Phe327=
NM_005347.5:c.981T>C MANE Select	NP_005338.1:p.Phe327=