Canonical Allele Identifier: CA477385711

Gene: HSPA8

Linked Data

• dbSNP Id: rs1865415426
• gnomAD v4: 11-123059230-C-T
• MyVariant Identifiers: chr11:g.122929938C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123059230C>T , CM000673.2:g.123059230C>T	GRCh38
NC_000011.9:g.122929938C>T , CM000673.1:g.122929938C>T	GRCh37
NC_000011.8:g.122435148C>T	NCBI36
NG_029473.1:g.7907G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1152G>A MANE Select	ENSP00000432083.1:p.Lys384=
ENST00000227378.7:c.1152G>A	ENSP00000227378.3:p.Lys384=
ENST00000453788.6:c.1152G>A	ENSP00000404372.2:p.Lys384=
ENST00000524552.5:c.-76G>A	ENSP00000435908.1:n.-76G>A
ENST00000526110.5:c.1095G>A	ENSP00000433584.1:p.Lys365=
ENST00000526862.1:n.430G>A
ENST00000532091.1:n.899G>A
ENST00000532636.5:c.1152G>A	ENSP00000437125.1:p.Lys384=
ENST00000533238.5:n.381-127G>A
ENST00000533540.5:c.714G>A	ENSP00000437189.1:p.Lys238=
ENST00000534319.5:c.444G>A	ENSP00000433316.1:p.Lys148=
ENST00000534624.5:c.1152G>A	ENSP00000432083.1:p.Lys384=
NM_006597.5:c.1152G>A	NP_006588.1:p.Lys384=
NM_153201.3:c.1152G>A	NP_694881.1:p.Lys384=
XM_011542798.1:c.1152G>A	XP_011541100.1:p.Lys384=
NM_006597.6:c.1152G>A MANE Select	NP_006588.1:p.Lys384=
NM_153201.4:c.1152G>A	NP_694881.1:p.Lys384=