Canonical Allele Identifier: CA1718330587

Gene: HSPB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.76303692T= , CM000669.2:g.76303692T=	GRCh38
NC_000007.13:g.75933009T= , CM000669.1:g.75933009T=	GRCh37
NC_000007.12:g.75770945T=	NCBI36
NG_008995.1:g.6135T= , LRG_248:g.6135T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248553.7:c.365-110T= MANE Select	ENSP00000248553.6:n.365-110T=
ENST00000674547.1:c.365-110T=	ENSP00000502461.1:n.365-110T=
ENST00000674638.1:c.365-115T=	ENSP00000502651.1:n.365-115T=
ENST00000674650.1:c.365-292T=	ENSP00000501628.1:n.365-292T=
ENST00000674965.1:c.365-85T=	ENSP00000501765.1:n.365-85T=
ENST00000675134.1:c.365-110T=	ENSP00000501831.1:n.365-110T=
ENST00000675226.1:c.369-115T=	ENSP00000502510.1:n.369-115T=
ENST00000675417.1:n.488T=
ENST00000675538.1:c.400-110T=	ENSP00000502495.1:n.400-110T=
ENST00000675733.1:n.405-70T=
ENST00000675906.1:c.365-110T=	ENSP00000502714.1:n.365-110T=
ENST00000676195.1:n.80+36T=
ENST00000676231.1:c.365-6T=	ENSP00000502249.1:n.365-6T=
ENST00000248553.6:c.365-110T=	ENSP00000248553.6:n.365-110T=
ENST00000429938.1:c.-176T=	ENSP00000405285.1:n.-176T=
ENST00000447574.1:c.*419T=	ENSP00000414357.1:n.*419T=
NM_001540.3:c.365-110T= , LRG_248t1:c.365-110T=	NP_001531.1:n.365-110T=
NM_001540.4:c.365-110T=	NP_001531.1:n.365-110T=
NM_001540.5:c.365-110T= MANE Select	NP_001531.1:n.365-110T=