Canonical Allele Identifier: CA383058598

Gene: HSPA8

Linked Data

• MyVariant Identifiers: chr11:g.122929961C>A (hg19) ; chr11:g.123059253C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123059253C>A , CM000673.2:g.123059253C>A	GRCh38
NC_000011.9:g.122929961C>A , CM000673.1:g.122929961C>A	GRCh37
NC_000011.8:g.122435171C>A	NCBI36
NG_029473.1:g.7884G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1129G>T MANE Select	ENSP00000432083.1:p.Ala377Ser
ENST00000227378.7:c.1129G>T	ENSP00000227378.3:p.Ala377Ser
ENST00000453788.6:c.1129G>T	ENSP00000404372.2:p.Ala377Ser
ENST00000524552.5:c.-99G>T	ENSP00000435908.1:n.-99G>T
ENST00000526110.5:c.1072G>T	ENSP00000433584.1:p.Ala358Ser
ENST00000526862.1:n.407G>T
ENST00000527983.5:n.1489G>T
ENST00000532091.1:n.876G>T
ENST00000532636.5:c.1129G>T	ENSP00000437125.1:p.Ala377Ser
ENST00000533238.5:n.381-150G>T
ENST00000533540.5:c.691G>T	ENSP00000437189.1:p.Ala231Ser
ENST00000534319.5:c.421G>T	ENSP00000433316.1:p.Ala141Ser
ENST00000534624.5:c.1129G>T	ENSP00000432083.1:p.Ala377Ser
NM_006597.5:c.1129G>T	NP_006588.1:p.Ala377Ser
NM_153201.3:c.1129G>T	NP_694881.1:p.Ala377Ser
XM_011542798.1:c.1129G>T	XP_011541100.1:p.Ala377Ser
NM_006597.6:c.1129G>T MANE Select	NP_006588.1:p.Ala377Ser
NM_153201.4:c.1129G>T	NP_694881.1:p.Ala377Ser