Canonical Allele Identifier: CA374897541

Gene: HSPA5

Linked Data

• gnomAD v4: 9-125238768-C-G
• MyVariant Identifiers: chr9:g.128001047C>G (hg19) ; chr9:g.125238768C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.125238768C>G , CM000671.2:g.125238768C>G	GRCh38
NC_000009.11:g.128001047C>G , CM000671.1:g.128001047C>G	GRCh37
NC_000009.10:g.127040868C>G	NCBI36
NG_027761.1:g.7620G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324460.7:c.1056G>C MANE Select	ENSP00000324173.6:p.Lys352Asn
ENST00000679355.1:n.1411G>C
ENST00000679475.1:n.1640G>C
ENST00000680032.1:c.1056G>C	ENSP00000506285.1:p.Lys352Asn
ENST00000680234.1:n.1312G>C
ENST00000680257.1:n.1312G>C
ENST00000680272.1:c.997-55G>C	ENSP00000506097.1:n.997-55G>C
ENST00000680494.1:n.2480G>C
ENST00000680640.1:n.2007G>C
ENST00000681045.1:n.1936G>C
ENST00000681424.1:n.1411G>C
ENST00000681540.1:n.1312G>C
ENST00000681544.1:n.1387G>C
ENST00000681675.1:n.1936G>C
ENST00000681774.1:n.2278G>C
ENST00000324460.6:c.1056G>C	ENSP00000324173.6:p.Lys352Asn
NM_005347.4:c.1056G>C	NP_005338.1:p.Lys352Asn
NM_005347.5:c.1056G>C MANE Select	NP_005338.1:p.Lys352Asn