Canonical Allele Identifier: CA1718331157

Gene: HSPB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.76303925G= , CM000669.2:g.76303925G=	GRCh38
NC_000007.13:g.75933242G= , CM000669.1:g.75933242G=	GRCh37
NC_000007.12:g.75771178G=	NCBI36
NG_008995.1:g.6368G= , LRG_248:g.6368G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248553.7:c.429-59G= MANE Select	ENSP00000248553.6:n.429-59G=
ENST00000674547.1:c.*19+37G=	ENSP00000502461.1:n.*19+37G=
ENST00000674638.1:c.424-59G=	ENSP00000502651.1:n.424-59G=
ENST00000674650.1:c.365-59G=	ENSP00000501628.1:n.365-59G=
ENST00000674965.1:c.*85-59G=	ENSP00000501765.1:n.*85-59G=
ENST00000675134.1:c.408-59G=	ENSP00000501831.1:n.408-59G=
ENST00000675226.1:c.428-59G=	ENSP00000502510.1:n.428-59G=
ENST00000675417.1:n.721G=
ENST00000675538.1:c.464-59G=	ENSP00000502495.1:n.464-59G=
ENST00000675906.1:c.*13+43G=	ENSP00000502714.1:n.*13+43G=
ENST00000676231.1:c.459-59G=	ENSP00000502249.1:n.459-59G=
ENST00000248553.6:c.429-59G=	ENSP00000248553.6:n.429-59G=
ENST00000429938.1:c.-76-59G=	ENSP00000405285.1:n.-76-59G=
ENST00000447574.1:c.*593-59G=	ENSP00000414357.1:n.*593-59G=
NM_001540.3:c.429-59G= , LRG_248t1:c.429-59G=	NP_001531.1:n.429-59G=
NM_001540.4:c.429-59G=	NP_001531.1:n.429-59G=
NM_001540.5:c.429-59G= MANE Select	NP_001531.1:n.429-59G=