Canonical Allele Identifier: CA477385744

Gene: HSPA8

Linked Data

• dbSNP Id: rs1163226600
• gnomAD v3: 11-123059149-A-G
• gnomAD v4: 11-123059149-A-G
• MyVariant Identifiers: chr11:g.122929857A>G (hg19) ; chr11:g.123059149A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123059149A>G , CM000673.2:g.123059149A>G	GRCh38
NC_000011.9:g.122929857A>G , CM000673.1:g.122929857A>G	GRCh37
NC_000011.8:g.122435067A>G	NCBI36
NG_029473.1:g.7988T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1233T>C MANE Select	ENSP00000432083.1:p.Thr411=
ENST00000227378.7:c.1233T>C	ENSP00000227378.3:p.Thr411=
ENST00000453788.6:c.1233T>C	ENSP00000404372.2:p.Thr411=
ENST00000524552.5:c.6T>C	ENSP00000435908.1:p.Thr2=
ENST00000526110.5:c.1176T>C	ENSP00000433584.1:p.Thr392=
ENST00000532091.1:n.980T>C
ENST00000532636.5:c.1233T>C	ENSP00000437125.1:p.Thr411=
ENST00000533238.5:n.381-46T>C
ENST00000533540.5:c.795T>C	ENSP00000437189.1:p.Thr265=
ENST00000534319.5:c.525T>C	ENSP00000433316.1:p.Thr175=
ENST00000534624.5:c.1233T>C	ENSP00000432083.1:p.Thr411=
NM_006597.5:c.1233T>C	NP_006588.1:p.Thr411=
NM_153201.3:c.1233T>C	NP_694881.1:p.Thr411=
XM_011542798.1:c.1233T>C	XP_011541100.1:p.Thr411=
NM_006597.6:c.1233T>C MANE Select	NP_006588.1:p.Thr411=
NM_153201.4:c.1233T>C	NP_694881.1:p.Thr411=