Canonical Allele Identifier: CA383058446

Gene: HSPA8

Linked Data

• MyVariant Identifiers: chr11:g.122929901T>A (hg19) ; chr11:g.123059193T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123059193T>A , CM000673.2:g.123059193T>A	GRCh38
NC_000011.9:g.122929901T>A , CM000673.1:g.122929901T>A	GRCh37
NC_000011.8:g.122435111T>A	NCBI36
NG_029473.1:g.7944A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1189A>T MANE Select	ENSP00000432083.1:p.Thr397Ser
ENST00000227378.7:c.1189A>T	ENSP00000227378.3:p.Thr397Ser
ENST00000453788.6:c.1189A>T	ENSP00000404372.2:p.Thr397Ser
ENST00000524552.5:c.-39A>T	ENSP00000435908.1:n.-39A>T
ENST00000526110.5:c.1132A>T	ENSP00000433584.1:p.Thr378Ser
ENST00000526862.1:n.467A>T
ENST00000532091.1:n.936A>T
ENST00000532636.5:c.1189A>T	ENSP00000437125.1:p.Thr397Ser
ENST00000533238.5:n.381-90A>T
ENST00000533540.5:c.751A>T	ENSP00000437189.1:p.Thr251Ser
ENST00000534319.5:c.481A>T	ENSP00000433316.1:p.Thr161Ser
ENST00000534624.5:c.1189A>T	ENSP00000432083.1:p.Thr397Ser
NM_006597.5:c.1189A>T	NP_006588.1:p.Thr397Ser
NM_153201.3:c.1189A>T	NP_694881.1:p.Thr397Ser
XM_011542798.1:c.1189A>T	XP_011541100.1:p.Thr397Ser
NM_006597.6:c.1189A>T MANE Select	NP_006588.1:p.Thr397Ser
NM_153201.4:c.1189A>T	NP_694881.1:p.Thr397Ser