Canonical Allele Identifier: CA1718330965

Gene: HSPB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.76303855C= , CM000669.2:g.76303855C=	GRCh38
NC_000007.13:g.75933172C= , CM000669.1:g.75933172C=	GRCh37
NC_000007.12:g.75771108C=	NCBI36
NG_008995.1:g.6298C= , LRG_248:g.6298C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248553.7:c.418C= MANE Select	ENSP00000248553.6:p.Arg140=
ENST00000674547.1:c.418C=	ENSP00000502461.1:p.Arg140=
ENST00000674638.1:c.413C=	ENSP00000502651.1:p.Ala138=
ENST00000674650.1:c.365-129C=	ENSP00000501628.1:n.365-129C=
ENST00000674965.1:c.*74C=	ENSP00000501765.1:n.*74C=
ENST00000675134.1:c.407+11C=	ENSP00000501831.1:n.407+11C=
ENST00000675226.1:c.417C=	ENSP00000502510.1:p.Arg139=
ENST00000675417.1:n.651C=
ENST00000675538.1:c.453C=	ENSP00000502495.1:p.Arg151=
ENST00000675906.1:c.418C=	ENSP00000502714.1:p.Arg140=
ENST00000676195.1:n.134C=
ENST00000676231.1:c.448C=	ENSP00000502249.1:p.Arg150=
ENST00000248553.6:c.418C=	ENSP00000248553.6:p.Arg140=
ENST00000429938.1:c.-87C=	ENSP00000405285.1:n.-87C=
ENST00000447574.1:c.*582C=	ENSP00000414357.1:n.*582C=
NM_001540.3:c.418C= , LRG_248t1:c.418C=	NP_001531.1:p.Arg140=
NM_001540.4:c.418C=	NP_001531.1:p.Arg140=
NM_001540.5:c.418C= MANE Select	NP_001531.1:p.Arg140=