Canonical Allele Identifier: CA6332495

Gene: HSPA8

Linked Data

• dbSNP Id: rs375700185
• ExAC: 11:122929570 G / T
• gnomAD v2: 11-122929570-G-T
• gnomAD v3: 11-123058862-G-T
• gnomAD v4: 11-123058862-G-T
• MyVariant Identifiers: chr11:g.122929570G>T (hg19) ; chr11:g.123058862G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123058862G>T , CM000673.2:g.123058862G>T	GRCh38
NC_000011.9:g.122929570G>T , CM000673.1:g.122929570G>T	GRCh37
NC_000011.8:g.122434780G>T	NCBI36
NG_029473.1:g.8275C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1324-32C>A MANE Select	ENSP00000432083.1:n.1324-32C>A
ENST00000227378.7:c.1324-32C>A	ENSP00000227378.3:n.1324-32C>A
ENST00000453788.6:c.1324-32C>A	ENSP00000404372.2:n.1324-32C>A
ENST00000524552.5:c.97-32C>A	ENSP00000435908.1:n.97-32C>A
ENST00000526110.5:c.1267-32C>A	ENSP00000433584.1:n.1267-32C>A
ENST00000526686.1:c.-53C>A	ENSP00000435019.1:n.-53C>A
ENST00000532091.1:n.1267C>A
ENST00000532636.5:c.1324-32C>A	ENSP00000437125.1:n.1324-32C>A
ENST00000533238.5:n.426-32C>A
ENST00000533540.5:c.886-32C>A	ENSP00000437189.1:n.886-32C>A
ENST00000534319.5:c.616-32C>A	ENSP00000433316.1:n.616-32C>A
ENST00000534624.5:c.1324-32C>A	ENSP00000432083.1:n.1324-32C>A
NM_006597.5:c.1324-32C>A	NP_006588.1:n.1324-32C>A
NM_153201.3:c.1324-32C>A	NP_694881.1:n.1324-32C>A
XM_011542798.1:c.1324-32C>A	XP_011541100.1:n.1324-32C>A
NM_006597.6:c.1324-32C>A MANE Select	NP_006588.1:n.1324-32C>A
NM_153201.4:c.1324-32C>A	NP_694881.1:n.1324-32C>A