Canonical Allele Identifier: CA383058435

Gene: HSPA8

Linked Data

• dbSNP Id: rs1395408526
• gnomAD v2: 11-122929898-G-A
• MyVariant Identifiers: chr11:g.122929898G>A (hg19) ; chr11:g.123059190G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123059190G>A , CM000673.2:g.123059190G>A	GRCh38
NC_000011.9:g.122929898G>A , CM000673.1:g.122929898G>A	GRCh37
NC_000011.8:g.122435108G>A	NCBI36
NG_029473.1:g.7947C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1192C>T MANE Select	ENSP00000432083.1:p.Pro398Ser
ENST00000227378.7:c.1192C>T	ENSP00000227378.3:p.Pro398Ser
ENST00000453788.6:c.1192C>T	ENSP00000404372.2:p.Pro398Ser
ENST00000524552.5:c.-36C>T	ENSP00000435908.1:n.-36C>T
ENST00000526110.5:c.1135C>T	ENSP00000433584.1:p.Pro379Ser
ENST00000526862.1:n.470C>T
ENST00000532091.1:n.939C>T
ENST00000532636.5:c.1192C>T	ENSP00000437125.1:p.Pro398Ser
ENST00000533238.5:n.381-87C>T
ENST00000533540.5:c.754C>T	ENSP00000437189.1:p.Pro252Ser
ENST00000534319.5:c.484C>T	ENSP00000433316.1:p.Pro162Ser
ENST00000534624.5:c.1192C>T	ENSP00000432083.1:p.Pro398Ser
NM_006597.5:c.1192C>T	NP_006588.1:p.Pro398Ser
NM_153201.3:c.1192C>T	NP_694881.1:p.Pro398Ser
XM_011542798.1:c.1192C>T	XP_011541100.1:p.Pro398Ser
NM_006597.6:c.1192C>T MANE Select	NP_006588.1:p.Pro398Ser
NM_153201.4:c.1192C>T	NP_694881.1:p.Pro398Ser