Canonical Allele Identifier: CA2580597837

Gene: HSPA5

Linked Data

• gnomAD v4: 9-125238840-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.125238840C>A , CM000671.2:g.125238840C>A	GRCh38
NC_000009.11:g.128001119C>A , CM000671.1:g.128001119C>A	GRCh37
NC_000009.10:g.127040940C>A	NCBI36
NG_027761.1:g.7548G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324460.7:c.997-13G>T MANE Select	ENSP00000324173.6:n.997-13G>T
ENST00000679355.1:n.1339G>T
ENST00000679475.1:n.1581-13G>T
ENST00000680032.1:c.997-13G>T	ENSP00000506285.1:n.997-13G>T
ENST00000680234.1:n.1253-13G>T
ENST00000680257.1:n.1253-13G>T
ENST00000680272.1:c.996+101G>T	ENSP00000506097.1:n.996+101G>T
ENST00000680494.1:n.2408G>T
ENST00000680640.1:n.1948-13G>T
ENST00000681045.1:n.1877-13G>T
ENST00000681424.1:n.1339G>T
ENST00000681540.1:n.1253-13G>T
ENST00000681544.1:n.1328-13G>T
ENST00000681675.1:n.1877-13G>T
ENST00000681774.1:n.2219-13G>T
ENST00000324460.6:c.997-13G>T	ENSP00000324173.6:n.997-13G>T
NM_005347.4:c.997-13G>T	NP_005338.1:n.997-13G>T
NM_005347.5:c.997-13G>T MANE Select	NP_005338.1:n.997-13G>T