Canonical Allele Identifier: CA1718331031

Gene: HSPB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.76303884T= , CM000669.2:g.76303884T=	GRCh38
NC_000007.13:g.75933201T= , CM000669.1:g.75933201T=	GRCh37
NC_000007.12:g.75771137T=	NCBI36
NG_008995.1:g.6327T= , LRG_248:g.6327T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248553.7:c.428+19T= MANE Select	ENSP00000248553.6:n.428+19T=
ENST00000674547.1:c.*15T=	ENSP00000502461.1:n.*15T=
ENST00000674638.1:c.423+19T=	ENSP00000502651.1:n.423+19T=
ENST00000674650.1:c.365-100T=	ENSP00000501628.1:n.365-100T=
ENST00000674965.1:c.*84+19T=	ENSP00000501765.1:n.*84+19T=
ENST00000675134.1:c.407+40T=	ENSP00000501831.1:n.407+40T=
ENST00000675226.1:c.427+19T=	ENSP00000502510.1:n.427+19T=
ENST00000675417.1:n.680T=
ENST00000675538.1:c.463+19T=	ENSP00000502495.1:n.463+19T=
ENST00000675906.1:c.*13+2T=	ENSP00000502714.1:n.*13+2T=
ENST00000676231.1:c.458+19T=	ENSP00000502249.1:n.458+19T=
ENST00000248553.6:c.428+19T=	ENSP00000248553.6:n.428+19T=
ENST00000429938.1:c.-77+19T=	ENSP00000405285.1:n.-77+19T=
ENST00000447574.1:c.*592+19T=	ENSP00000414357.1:n.*592+19T=
NM_001540.3:c.428+19T= , LRG_248t1:c.428+19T=	NP_001531.1:n.428+19T=
NM_001540.4:c.428+19T=	NP_001531.1:n.428+19T=
NM_001540.5:c.428+19T= MANE Select	NP_001531.1:n.428+19T=