Canonical Allele Identifier: CA6332444

Gene: HSPA8

Linked Data

• dbSNP Id: rs374190356
• ExAC: 11:122929243 G / T
• gnomAD v2: 11-122929243-G-T
• gnomAD v3: 11-123058535-G-T
• gnomAD v4: 11-123058535-G-T
• MyVariant Identifiers: chr11:g.122929243G>T (hg19) ; chr11:g.123058535G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123058535G>T , CM000673.2:g.123058535G>T	GRCh38
NC_000011.9:g.122929243G>T , CM000673.1:g.122929243G>T	GRCh37
NC_000011.8:g.122434453G>T	NCBI36
NG_029473.1:g.8602C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1523-51C>A MANE Select	ENSP00000432083.1:n.1523-51C>A
ENST00000227378.7:c.1523-51C>A	ENSP00000227378.3:n.1523-51C>A
ENST00000453788.6:c.1387+232C>A	ENSP00000404372.2:n.1387+232C>A
ENST00000524552.5:c.296-51C>A	ENSP00000435908.1:n.296-51C>A
ENST00000526110.5:c.1466-51C>A	ENSP00000433584.1:n.1466-51C>A
ENST00000526686.1:c.179-51C>A	ENSP00000435019.1:n.179-51C>A
ENST00000532091.1:n.1594C>A
ENST00000532636.5:c.1523-51C>A	ENSP00000437125.1:n.1523-51C>A
ENST00000533540.5:c.1085-51C>A	ENSP00000437189.1:n.1085-51C>A
ENST00000534319.5:c.815-51C>A	ENSP00000433316.1:n.815-51C>A
ENST00000534624.5:c.1523-51C>A	ENSP00000432083.1:n.1523-51C>A
NM_006597.5:c.1523-51C>A	NP_006588.1:n.1523-51C>A
NM_153201.3:c.1387+232C>A	NP_694881.1:n.1387+232C>A
XM_011542798.1:c.1523-51C>A	XP_011541100.1:n.1523-51C>A
NM_006597.6:c.1523-51C>A MANE Select	NP_006588.1:n.1523-51C>A
NM_153201.4:c.1387+232C>A	NP_694881.1:n.1387+232C>A