Canonical Allele Identifier: CA6332558

Gene: HSPA8

Linked Data

• dbSNP Id: rs746921647
• ExAC: 11:122929997 G / T
• gnomAD v2: 11-122929997-G-T
• gnomAD v3: 11-123059289-G-T
• gnomAD v4: 11-123059289-G-T
• MyVariant Identifiers: chr11:g.122929997G>T (hg19) ; chr11:g.122929997_122930002delinsTAAGTT (hg19) ; chr11:g.123059289G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123059289G>T , CM000673.2:g.123059289G>T	GRCh38
NC_000011.9:g.122929997G>T , CM000673.1:g.122929997G>T	GRCh37
NC_000011.8:g.122435207G>T	NCBI36
NG_029473.1:g.7848C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1121-28C>A MANE Select	ENSP00000432083.1:n.1121-28C>A
ENST00000227378.7:c.1121-28C>A	ENSP00000227378.3:n.1121-28C>A
ENST00000453788.6:c.1121-28C>A	ENSP00000404372.2:n.1121-28C>A
ENST00000524552.5:c.-135C>A	ENSP00000435908.1:n.-135C>A
ENST00000526110.5:c.1064-28C>A	ENSP00000433584.1:n.1064-28C>A
ENST00000526862.1:n.399-28C>A
ENST00000527983.5:n.1453C>A
ENST00000532091.1:n.868-28C>A
ENST00000532636.5:c.1121-28C>A	ENSP00000437125.1:n.1121-28C>A
ENST00000533238.5:n.381-186C>A
ENST00000533540.5:c.683-28C>A	ENSP00000437189.1:n.683-28C>A
ENST00000534319.5:c.413-28C>A	ENSP00000433316.1:n.413-28C>A
ENST00000534624.5:c.1121-28C>A	ENSP00000432083.1:n.1121-28C>A
NM_006597.5:c.1121-28C>A	NP_006588.1:n.1121-28C>A
NM_153201.3:c.1121-28C>A	NP_694881.1:n.1121-28C>A
XM_011542798.1:c.1121-28C>A	XP_011541100.1:n.1121-28C>A
NM_006597.6:c.1121-28C>A MANE Select	NP_006588.1:n.1121-28C>A
NM_153201.4:c.1121-28C>A	NP_694881.1:n.1121-28C>A