Canonical Allele Identifier: CA383058609

Gene: HSPA8

Linked Data

• MyVariant Identifiers: chr11:g.122929966A>T (hg19) ; chr11:g.123059258A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123059258A>T , CM000673.2:g.123059258A>T	GRCh38
NC_000011.9:g.122929966A>T , CM000673.1:g.122929966A>T	GRCh37
NC_000011.8:g.122435176A>T	NCBI36
NG_029473.1:g.7879T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1124T>A MANE Select	ENSP00000432083.1:p.Val375Asp
ENST00000227378.7:c.1124T>A	ENSP00000227378.3:p.Val375Asp
ENST00000453788.6:c.1124T>A	ENSP00000404372.2:p.Val375Asp
ENST00000524552.5:c.-104T>A	ENSP00000435908.1:n.-104T>A
ENST00000526110.5:c.1067T>A	ENSP00000433584.1:p.Val356Asp
ENST00000526862.1:n.402T>A
ENST00000527983.5:n.1484T>A
ENST00000532091.1:n.871T>A
ENST00000532636.5:c.1124T>A	ENSP00000437125.1:p.Val375Asp
ENST00000533238.5:n.381-155T>A
ENST00000533540.5:c.686T>A	ENSP00000437189.1:p.Val229Asp
ENST00000534319.5:c.416T>A	ENSP00000433316.1:p.Val139Asp
ENST00000534624.5:c.1124T>A	ENSP00000432083.1:p.Val375Asp
NM_006597.5:c.1124T>A	NP_006588.1:p.Val375Asp
NM_153201.3:c.1124T>A	NP_694881.1:p.Val375Asp
XM_011542798.1:c.1124T>A	XP_011541100.1:p.Val375Asp
NM_006597.6:c.1124T>A MANE Select	NP_006588.1:p.Val375Asp
NM_153201.4:c.1124T>A	NP_694881.1:p.Val375Asp