Canonical Allele Identifier: CA1718330969

Gene: HSPB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.76303857G= , CM000669.2:g.76303857G=	GRCh38
NC_000007.13:g.75933174G= , CM000669.1:g.75933174G=	GRCh37
NC_000007.12:g.75771110G=	NCBI36
NG_008995.1:g.6300G= , LRG_248:g.6300G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248553.7:c.420G= MANE Select	ENSP00000248553.6:p.Arg140=
ENST00000674547.1:c.420G=	ENSP00000502461.1:p.Arg140=
ENST00000674638.1:c.415G=	ENSP00000502651.1:p.Glu139=
ENST00000674650.1:c.365-127G=	ENSP00000501628.1:n.365-127G=
ENST00000674965.1:c.*76G=	ENSP00000501765.1:n.*76G=
ENST00000675134.1:c.407+13G=	ENSP00000501831.1:n.407+13G=
ENST00000675226.1:c.419G=	ENSP00000502510.1:p.Gly140=
ENST00000675417.1:n.653G=
ENST00000675538.1:c.455G=	ENSP00000502495.1:p.Gly152=
ENST00000675906.1:c.420G=	ENSP00000502714.1:p.Arg140=
ENST00000676195.1:n.136G=
ENST00000676231.1:c.450G=	ENSP00000502249.1:p.Arg150=
ENST00000248553.6:c.420G=	ENSP00000248553.6:p.Arg140=
ENST00000429938.1:c.-85G=	ENSP00000405285.1:n.-85G=
ENST00000447574.1:c.*584G=	ENSP00000414357.1:n.*584G=
NM_001540.3:c.420G= , LRG_248t1:c.420G=	NP_001531.1:p.Arg140=
NM_001540.4:c.420G=	NP_001531.1:p.Arg140=
NM_001540.5:c.420G= MANE Select	NP_001531.1:p.Arg140=