Canonical Allele Identifier: CA477385391

Gene: HSPA8

Linked Data

• MyVariant Identifiers: chr11:g.122929536A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123058828A>G , CM000673.2:g.123058828A>G	GRCh38
NC_000011.9:g.122929536A>G , CM000673.1:g.122929536A>G	GRCh37
NC_000011.8:g.122434746A>G	NCBI36
NG_029473.1:g.8309T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000534624.6:c.1326T>C MANE Select	ENSP00000432083.1:p.Val442=
ENST00000227378.7:c.1326T>C	ENSP00000227378.3:p.Val442=
ENST00000453788.6:c.1326T>C	ENSP00000404372.2:p.Val442=
ENST00000524552.5:c.99T>C	ENSP00000435908.1:p.Val33=
ENST00000526110.5:c.1269T>C	ENSP00000433584.1:p.Val423=
ENST00000526686.1:c.-19T>C	ENSP00000435019.1:n.-19T>C
ENST00000532091.1:n.1301T>C
ENST00000532636.5:c.1326T>C	ENSP00000437125.1:p.Val442=
ENST00000533238.5:n.428T>C
ENST00000533540.5:c.888T>C	ENSP00000437189.1:p.Val296=
ENST00000534319.5:c.618T>C	ENSP00000433316.1:p.Val206=
ENST00000534624.5:c.1326T>C	ENSP00000432083.1:p.Val442=
NM_006597.5:c.1326T>C	NP_006588.1:p.Val442=
NM_153201.3:c.1326T>C	NP_694881.1:p.Val442=
XM_011542798.1:c.1326T>C	XP_011541100.1:p.Val442=
NM_006597.6:c.1326T>C MANE Select	NP_006588.1:p.Val442=
NM_153201.4:c.1326T>C	NP_694881.1:p.Val442=