Canonical Allele Identifier: CA6332482

Gene: HSPA8

Linked Data

• dbSNP Id: rs767284605
• ExAC: 11:122929527 G / A
• gnomAD v2: 11-122929527-G-A
• gnomAD v3: 11-123058819-G-A
• gnomAD v4: 11-123058819-G-A
• MyVariant Identifiers: chr11:g.122929527G>A (hg19) ; chr11:g.123058819G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123058819G>A , CM000673.2:g.123058819G>A	GRCh38
NC_000011.9:g.122929527G>A , CM000673.1:g.122929527G>A	GRCh37
NC_000011.8:g.122434737G>A	NCBI36
NG_029473.1:g.8318C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000534624.6:c.1335C>T MANE Select	ENSP00000432083.1:p.Gly445=
ENST00000227378.7:c.1335C>T	ENSP00000227378.3:p.Gly445=
ENST00000453788.6:c.1335C>T	ENSP00000404372.2:p.Gly445=
ENST00000524552.5:c.108C>T	ENSP00000435908.1:p.Gly36=
ENST00000526110.5:c.1278C>T	ENSP00000433584.1:p.Gly426=
ENST00000526686.1:c.-10C>T	ENSP00000435019.1:n.-10C>T
ENST00000532091.1:n.1310C>T
ENST00000532636.5:c.1335C>T	ENSP00000437125.1:p.Gly445=
ENST00000533238.5:n.437C>T
ENST00000533540.5:c.897C>T	ENSP00000437189.1:p.Gly299=
ENST00000534319.5:c.627C>T	ENSP00000433316.1:p.Gly209=
ENST00000534624.5:c.1335C>T	ENSP00000432083.1:p.Gly445=
NM_006597.5:c.1335C>T	NP_006588.1:p.Gly445=
NM_153201.3:c.1335C>T	NP_694881.1:p.Gly445=
XM_011542798.1:c.1335C>T	XP_011541100.1:p.Gly445=
NM_006597.6:c.1335C>T MANE Select	NP_006588.1:p.Gly445=
NM_153201.4:c.1335C>T	NP_694881.1:p.Gly445=