Canonical Allele Identifier: CA1718330929

Gene: HSPB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.76303845G= , CM000669.2:g.76303845G=	GRCh38
NC_000007.13:g.75933162G= , CM000669.1:g.75933162G=	GRCh37
NC_000007.12:g.75771098G=	NCBI36
NG_008995.1:g.6288G= , LRG_248:g.6288G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248553.7:c.408G= MANE Select	ENSP00000248553.6:p.Arg136=
ENST00000674547.1:c.408G=	ENSP00000502461.1:p.Arg136=
ENST00000674638.1:c.403G=	ENSP00000502651.1:p.Val135=
ENST00000674650.1:c.365-139G=	ENSP00000501628.1:n.365-139G=
ENST00000674965.1:c.*64G=	ENSP00000501765.1:n.*64G=
ENST00000675134.1:c.407+1G=	ENSP00000501831.1:n.407+1G=
ENST00000675226.1:c.407G=	ENSP00000502510.1:p.Gly136=
ENST00000675417.1:n.641G=
ENST00000675538.1:c.443G=	ENSP00000502495.1:p.Gly148=
ENST00000675906.1:c.408G=	ENSP00000502714.1:p.Arg136=
ENST00000676195.1:n.124G=
ENST00000676231.1:c.438G=	ENSP00000502249.1:p.Arg146=
ENST00000248553.6:c.408G=	ENSP00000248553.6:p.Arg136=
ENST00000429938.1:c.-97G=	ENSP00000405285.1:n.-97G=
ENST00000447574.1:c.*572G=	ENSP00000414357.1:n.*572G=
NM_001540.3:c.408G= , LRG_248t1:c.408G=	NP_001531.1:p.Arg136=
NM_001540.4:c.408G=	NP_001531.1:p.Arg136=
NM_001540.5:c.408G= MANE Select	NP_001531.1:p.Arg136=