Canonical Allele Identifier: CA6332539

Gene: HSPA8

Linked Data

• dbSNP Id: rs775435579
• ExAC: 11:122929965 G / T
• gnomAD v2: 11-122929965-G-T
• gnomAD v3: 11-123059257-G-T
• gnomAD v4: 11-123059257-G-T
• MyVariant Identifiers: chr11:g.122929965G>T (hg19) ; chr11:g.123059257G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123059257G>T , CM000673.2:g.123059257G>T	GRCh38
NC_000011.9:g.122929965G>T , CM000673.1:g.122929965G>T	GRCh37
NC_000011.8:g.122435175G>T	NCBI36
NG_029473.1:g.7880C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1125C>A MANE Select	ENSP00000432083.1:p.Val375=
ENST00000227378.7:c.1125C>A	ENSP00000227378.3:p.Val375=
ENST00000453788.6:c.1125C>A	ENSP00000404372.2:p.Val375=
ENST00000524552.5:c.-103C>A	ENSP00000435908.1:n.-103C>A
ENST00000526110.5:c.1068C>A	ENSP00000433584.1:p.Val356=
ENST00000526862.1:n.403C>A
ENST00000527983.5:n.1485C>A
ENST00000532091.1:n.872C>A
ENST00000532636.5:c.1125C>A	ENSP00000437125.1:p.Val375=
ENST00000533238.5:n.381-154C>A
ENST00000533540.5:c.687C>A	ENSP00000437189.1:p.Val229=
ENST00000534319.5:c.417C>A	ENSP00000433316.1:p.Val139=
ENST00000534624.5:c.1125C>A	ENSP00000432083.1:p.Val375=
NM_006597.5:c.1125C>A	NP_006588.1:p.Val375=
NM_153201.3:c.1125C>A	NP_694881.1:p.Val375=
XM_011542798.1:c.1125C>A	XP_011541100.1:p.Val375=
NM_006597.6:c.1125C>A MANE Select	NP_006588.1:p.Val375=
NM_153201.4:c.1125C>A	NP_694881.1:p.Val375=