Canonical Allele Identifier: CA383057296

Gene: HSPA8

Linked Data

• MyVariant Identifiers: chr11:g.122929448G>A (hg19) ; chr11:g.123058740G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123058740G>A , CM000673.2:g.123058740G>A	GRCh38
NC_000011.9:g.122929448G>A , CM000673.1:g.122929448G>A	GRCh37
NC_000011.8:g.122434658G>A	NCBI36
NG_029473.1:g.8397C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1414C>T MANE Select	ENSP00000432083.1:p.Pro472Ser
ENST00000227378.7:c.1414C>T	ENSP00000227378.3:p.Pro472Ser
ENST00000453788.6:c.1387+27C>T	ENSP00000404372.2:n.1387+27C>T
ENST00000524552.5:c.187C>T	ENSP00000435908.1:p.Pro63Ser
ENST00000526110.5:c.1357C>T	ENSP00000433584.1:p.Pro453Ser
ENST00000526686.1:c.70C>T	ENSP00000435019.1:p.Pro24Ser
ENST00000532091.1:n.1389C>T
ENST00000532636.5:c.1414C>T	ENSP00000437125.1:p.Pro472Ser
ENST00000533540.5:c.976C>T	ENSP00000437189.1:p.Pro326Ser
ENST00000534319.5:c.706C>T	ENSP00000433316.1:p.Pro236Ser
ENST00000534624.5:c.1414C>T	ENSP00000432083.1:p.Pro472Ser
NM_006597.5:c.1414C>T	NP_006588.1:p.Pro472Ser
NM_153201.3:c.1387+27C>T	NP_694881.1:n.1387+27C>T
XM_011542798.1:c.1414C>T	XP_011541100.1:p.Pro472Ser
NM_006597.6:c.1414C>T MANE Select	NP_006588.1:p.Pro472Ser
NM_153201.4:c.1387+27C>T	NP_694881.1:n.1387+27C>T