Canonical Allele Identifier: CA13537036

Gene: HSPA8

Linked Data

• dbSNP Id: rs2276077
• gnomAD v2: 11-122932817-C-T
• gnomAD v3: 11-123062109-C-T
• gnomAD v4: 11-123062109-C-T
• MyVariant Identifiers: chr11:g.122932817C>T (hg19) ; chr11:g.123062109C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123062109C>T , CM000673.2:g.123062109C>T	GRCh38
NC_000011.9:g.122932817C>T , CM000673.1:g.122932817C>T	GRCh37
NC_000011.8:g.122438027C>T	NCBI36
NG_029473.1:g.5028G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000534624.6:c.-51G>A MANE Select	ENSP00000432083.1:n.-51G>A
ENST00000453788.6:c.-51G>A	ENSP00000404372.2:n.-51G>A
ENST00000525463.5:c.-51G>A	ENSP00000436762.1:n.-51G>A
ENST00000525624.5:c.-6+641G>A	ENSP00000435154.1:n.-6+641G>A
ENST00000527387.5:c.-6+204G>A	ENSP00000436183.1:n.-6+204G>A
ENST00000527983.5:n.99G>A
ENST00000528292.5:c.-160G>A	ENSP00000432884.1:n.-160G>A
ENST00000531063.1:n.28G>A
ENST00000532167.5:n.28G>A
ENST00000532780.5:n.323+238G>A
ENST00000533238.5:n.31G>A
ENST00000533540.5:c.-51G>A	ENSP00000437189.1:n.-51G>A
ENST00000534624.5:c.-51G>A	ENSP00000432083.1:n.-51G>A
NM_006597.5:c.-51G>A	NP_006588.1:n.-51G>A
NM_153201.3:c.-51G>A	NP_694881.1:n.-51G>A
XM_011542798.1:c.-6+238G>A	XP_011541100.1:n.-6+238G>A
NM_006597.6:c.-51G>A MANE Select	NP_006588.1:n.-51G>A
NM_153201.4:c.-51G>A	NP_694881.1:n.-51G>A