Canonical Allele Identifier: CA1718330695

Gene: HSPB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.76303772C= , CM000669.2:g.76303772C=	GRCh38
NC_000007.13:g.75933089C= , CM000669.1:g.75933089C=	GRCh37
NC_000007.12:g.75771025C=	NCBI36
NG_008995.1:g.6215C= , LRG_248:g.6215C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248553.7:c.365-30C= MANE Select	ENSP00000248553.6:n.365-30C=
ENST00000674547.1:c.365-30C=	ENSP00000502461.1:n.365-30C=
ENST00000674638.1:c.365-35C=	ENSP00000502651.1:n.365-35C=
ENST00000674650.1:c.365-212C=	ENSP00000501628.1:n.365-212C=
ENST00000674965.1:c.365-5C=	ENSP00000501765.1:n.365-5C=
ENST00000675134.1:c.365-30C=	ENSP00000501831.1:n.365-30C=
ENST00000675226.1:c.369-35C=	ENSP00000502510.1:n.369-35C=
ENST00000675417.1:n.568C=
ENST00000675538.1:c.400-30C=	ENSP00000502495.1:n.400-30C=
ENST00000675733.1:n.415C=
ENST00000675906.1:c.365-30C=	ENSP00000502714.1:n.365-30C=
ENST00000676195.1:n.81-30C=
ENST00000676231.1:c.395-30C=	ENSP00000502249.1:n.395-30C=
ENST00000248553.6:c.365-30C=	ENSP00000248553.6:n.365-30C=
ENST00000429938.1:c.-140-30C=	ENSP00000405285.1:n.-140-30C=
ENST00000447574.1:c.*499C=	ENSP00000414357.1:n.*499C=
NM_001540.3:c.365-30C= , LRG_248t1:c.365-30C=	NP_001531.1:n.365-30C=
NM_001540.4:c.365-30C=	NP_001531.1:n.365-30C=
NM_001540.5:c.365-30C= MANE Select	NP_001531.1:n.365-30C=