Canonical Allele Identifier: CA383056930

Gene: HSPA8

Linked Data

• MyVariant Identifiers: chr11:g.122929176T>G (hg19) ; chr11:g.123058468T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123058468T>G , CM000673.2:g.123058468T>G	GRCh38
NC_000011.9:g.122929176T>G , CM000673.1:g.122929176T>G	GRCh37
NC_000011.8:g.122434386T>G	NCBI36
NG_029473.1:g.8669A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1539A>C MANE Select	ENSP00000432083.1:p.Glu513Asp
ENST00000227378.7:c.1539A>C	ENSP00000227378.3:p.Glu513Asp
ENST00000453788.6:c.1387+299A>C	ENSP00000404372.2:n.1387+299A>C
ENST00000524552.5:c.312A>C	ENSP00000435908.1:p.Glu104Asp
ENST00000526110.5:c.1482A>C	ENSP00000433584.1:p.Glu494Asp
ENST00000526686.1:c.195A>C	ENSP00000435019.1:p.Glu65Asp
ENST00000532091.1:n.1661A>C
ENST00000532636.5:c.1539A>C	ENSP00000437125.1:p.Glu513Asp
ENST00000533540.5:c.1101A>C	ENSP00000437189.1:p.Glu367Asp
ENST00000534319.5:c.831A>C	ENSP00000433316.1:p.Glu277Asp
ENST00000534624.5:c.1539A>C	ENSP00000432083.1:p.Glu513Asp
NM_006597.5:c.1539A>C	NP_006588.1:p.Glu513Asp
NM_153201.3:c.1387+299A>C	NP_694881.1:n.1387+299A>C
XM_011542798.1:c.1539A>C	XP_011541100.1:p.Glu513Asp
NM_006597.6:c.1539A>C MANE Select	NP_006588.1:p.Glu513Asp
NM_153201.4:c.1387+299A>C	NP_694881.1:n.1387+299A>C