Canonical Allele Identifier: CA1129088040

Gene: HSPA5

Linked Data

• dbSNP Id: rs1832528472
• gnomAD v3: 9-125238839-A-G
• gnomAD v4: 9-125238839-A-G

Genomic Alleles

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

Transcript Alleles

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