Canonical Allele Identifier: CA383057252

Gene: HSPA8

Linked Data

• MyVariant Identifiers: chr11:g.122929429A>G (hg19) ; chr11:g.123058721A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123058721A>G , CM000673.2:g.123058721A>G	GRCh38
NC_000011.9:g.122929429A>G , CM000673.1:g.122929429A>G	GRCh37
NC_000011.8:g.122434639A>G	NCBI36
NG_029473.1:g.8416T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1433T>C MANE Select	ENSP00000432083.1:p.Phe478Ser
ENST00000227378.7:c.1433T>C	ENSP00000227378.3:p.Phe478Ser
ENST00000453788.6:c.1387+46T>C	ENSP00000404372.2:n.1387+46T>C
ENST00000524552.5:c.206T>C	ENSP00000435908.1:p.Phe69Ser
ENST00000526110.5:c.1376T>C	ENSP00000433584.1:p.Phe459Ser
ENST00000526686.1:c.89T>C	ENSP00000435019.1:p.Phe30Ser
ENST00000532091.1:n.1408T>C
ENST00000532636.5:c.1433T>C	ENSP00000437125.1:p.Phe478Ser
ENST00000533540.5:c.995T>C	ENSP00000437189.1:p.Phe332Ser
ENST00000534319.5:c.725T>C	ENSP00000433316.1:p.Phe242Ser
ENST00000534624.5:c.1433T>C	ENSP00000432083.1:p.Phe478Ser
NM_006597.5:c.1433T>C	NP_006588.1:p.Phe478Ser
NM_153201.3:c.1387+46T>C	NP_694881.1:n.1387+46T>C
XM_011542798.1:c.1433T>C	XP_011541100.1:p.Phe478Ser
NM_006597.6:c.1433T>C MANE Select	NP_006588.1:p.Phe478Ser
NM_153201.4:c.1387+46T>C	NP_694881.1:n.1387+46T>C