Canonical Allele Identifier: CA383058490

Gene: HSPA8

Linked Data

• MyVariant Identifiers: chr11:g.122929913G>A (hg19) ; chr11:g.123059205G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123059205G>A , CM000673.2:g.123059205G>A	GRCh38
NC_000011.9:g.122929913G>A , CM000673.1:g.122929913G>A	GRCh37
NC_000011.8:g.122435123G>A	NCBI36
NG_029473.1:g.7932C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1177C>T MANE Select	ENSP00000432083.1:p.Leu393Phe
ENST00000227378.7:c.1177C>T	ENSP00000227378.3:p.Leu393Phe
ENST00000453788.6:c.1177C>T	ENSP00000404372.2:p.Leu393Phe
ENST00000524552.5:c.-51C>T	ENSP00000435908.1:n.-51C>T
ENST00000526110.5:c.1120C>T	ENSP00000433584.1:p.Leu374Phe
ENST00000526862.1:n.455C>T
ENST00000532091.1:n.924C>T
ENST00000532636.5:c.1177C>T	ENSP00000437125.1:p.Leu393Phe
ENST00000533238.5:n.381-102C>T
ENST00000533540.5:c.739C>T	ENSP00000437189.1:p.Leu247Phe
ENST00000534319.5:c.469C>T	ENSP00000433316.1:p.Leu157Phe
ENST00000534624.5:c.1177C>T	ENSP00000432083.1:p.Leu393Phe
NM_006597.5:c.1177C>T	NP_006588.1:p.Leu393Phe
NM_153201.3:c.1177C>T	NP_694881.1:p.Leu393Phe
XM_011542798.1:c.1177C>T	XP_011541100.1:p.Leu393Phe
NM_006597.6:c.1177C>T MANE Select	NP_006588.1:p.Leu393Phe
NM_153201.4:c.1177C>T	NP_694881.1:p.Leu393Phe