Canonical Allele Identifier: CA5239703

Gene: HSPA5

Linked Data

• dbSNP Id: rs748080410
• ExAC: 9:128001208 C / T
• gnomAD v2: 9-128001208-C-T
• gnomAD v3: 9-125238929-C-T
• gnomAD v4: 9-125238929-C-T
• MyVariant Identifiers: chr9:g.128001208C>T (hg19) ; chr9:g.125238929C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.125238929C>T , CM000671.2:g.125238929C>T	GRCh38
NC_000009.11:g.128001208C>T , CM000671.1:g.128001208C>T	GRCh37
NC_000009.10:g.127041029C>T	NCBI36
NG_027761.1:g.7459G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324460.7:c.996+12G>A MANE Select	ENSP00000324173.6:n.996+12G>A
ENST00000679355.1:n.1250G>A
ENST00000679475.1:n.1580+12G>A
ENST00000680032.1:c.996+12G>A	ENSP00000506285.1:n.996+12G>A
ENST00000680234.1:n.1252+12G>A
ENST00000680257.1:n.1252+12G>A
ENST00000680272.1:c.996+12G>A	ENSP00000506097.1:n.996+12G>A
ENST00000680494.1:n.2319G>A
ENST00000680640.1:n.1947+12G>A
ENST00000681045.1:n.1876+12G>A
ENST00000681424.1:n.1250G>A
ENST00000681540.1:n.1252+12G>A
ENST00000681544.1:n.1327+12G>A
ENST00000681675.1:n.1876+12G>A
ENST00000681774.1:n.2218+12G>A
ENST00000324460.6:c.996+12G>A	ENSP00000324173.6:n.996+12G>A
NM_005347.4:c.996+12G>A	NP_005338.1:n.996+12G>A
NM_005347.5:c.996+12G>A MANE Select	NP_005338.1:n.996+12G>A