Canonical Allele Identifier: CA1718331055

Gene: HSPB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.76303888G= , CM000669.2:g.76303888G=	GRCh38
NC_000007.13:g.75933205G= , CM000669.1:g.75933205G=	GRCh37
NC_000007.12:g.75771141G=	NCBI36
NG_008995.1:g.6331G= , LRG_248:g.6331G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248553.7:c.428+23G= MANE Select	ENSP00000248553.6:n.428+23G=
ENST00000674547.1:c.*19G=	ENSP00000502461.1:n.*19G=
ENST00000674638.1:c.423+23G=	ENSP00000502651.1:n.423+23G=
ENST00000674650.1:c.365-96G=	ENSP00000501628.1:n.365-96G=
ENST00000674965.1:c.*84+23G=	ENSP00000501765.1:n.*84+23G=
ENST00000675134.1:c.407+44G=	ENSP00000501831.1:n.407+44G=
ENST00000675226.1:c.427+23G=	ENSP00000502510.1:n.427+23G=
ENST00000675417.1:n.684G=
ENST00000675538.1:c.463+23G=	ENSP00000502495.1:n.463+23G=
ENST00000675906.1:c.*13+6G=	ENSP00000502714.1:n.*13+6G=
ENST00000676231.1:c.458+23G=	ENSP00000502249.1:n.458+23G=
ENST00000248553.6:c.428+23G=	ENSP00000248553.6:n.428+23G=
ENST00000429938.1:c.-77+23G=	ENSP00000405285.1:n.-77+23G=
ENST00000447574.1:c.*592+23G=	ENSP00000414357.1:n.*592+23G=
NM_001540.3:c.428+23G= , LRG_248t1:c.428+23G=	NP_001531.1:n.428+23G=
NM_001540.4:c.428+23G=	NP_001531.1:n.428+23G=
NM_001540.5:c.428+23G= MANE Select	NP_001531.1:n.428+23G=