Canonical Allele Identifier: CA1129088074

Gene: HSPA5

Linked Data

• dbSNP Id: rs1832529879
• gnomAD v3: 9-125238903-G-A
• gnomAD v4: 9-125238903-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.125238903G>A , CM000671.2:g.125238903G>A	GRCh38
NC_000009.11:g.128001182G>A , CM000671.1:g.128001182G>A	GRCh37
NC_000009.10:g.127041003G>A	NCBI36
NG_027761.1:g.7485C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324460.7:c.996+38C>T MANE Select	ENSP00000324173.6:n.996+38C>T
ENST00000679355.1:n.1276C>T
ENST00000679475.1:n.1580+38C>T
ENST00000680032.1:c.996+38C>T	ENSP00000506285.1:n.996+38C>T
ENST00000680234.1:n.1252+38C>T
ENST00000680257.1:n.1252+38C>T
ENST00000680272.1:c.996+38C>T	ENSP00000506097.1:n.996+38C>T
ENST00000680494.1:n.2345C>T
ENST00000680640.1:n.1947+38C>T
ENST00000681045.1:n.1876+38C>T
ENST00000681424.1:n.1276C>T
ENST00000681540.1:n.1252+38C>T
ENST00000681544.1:n.1327+38C>T
ENST00000681675.1:n.1876+38C>T
ENST00000681774.1:n.2218+38C>T
ENST00000324460.6:c.996+38C>T	ENSP00000324173.6:n.996+38C>T
NM_005347.4:c.996+38C>T	NP_005338.1:n.996+38C>T
NM_005347.5:c.996+38C>T MANE Select	NP_005338.1:n.996+38C>T