Canonical Allele Identifier: CA1718330982

Gene: HSPB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.76303863C= , CM000669.2:g.76303863C=	GRCh38
NC_000007.13:g.75933180C= , CM000669.1:g.75933180C=	GRCh37
NC_000007.12:g.75771116C=	NCBI36
NG_008995.1:g.6306C= , LRG_248:g.6306C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248553.7:c.426C= MANE Select	ENSP00000248553.6:p.Tyr142=
ENST00000674547.1:c.426C=	ENSP00000502461.1:p.Tyr142=
ENST00000674638.1:c.421C=	ENSP00000502651.1:p.His141=
ENST00000674650.1:c.365-121C=	ENSP00000501628.1:n.365-121C=
ENST00000674965.1:c.*82C=	ENSP00000501765.1:n.*82C=
ENST00000675134.1:c.407+19C=	ENSP00000501831.1:n.407+19C=
ENST00000675226.1:c.425C=	ENSP00000502510.1:p.Thr142=
ENST00000675417.1:n.659C=
ENST00000675538.1:c.461C=	ENSP00000502495.1:p.Thr154=
ENST00000675906.1:c.426C=	ENSP00000502714.1:p.Tyr142=
ENST00000676195.1:n.142C=
ENST00000676231.1:c.456C=	ENSP00000502249.1:p.Tyr152=
ENST00000248553.6:c.426C=	ENSP00000248553.6:p.Tyr142=
ENST00000429938.1:c.-79C=	ENSP00000405285.1:n.-79C=
ENST00000447574.1:c.*590C=	ENSP00000414357.1:n.*590C=
NM_001540.3:c.426C= , LRG_248t1:c.426C=	NP_001531.1:p.Tyr142=
NM_001540.4:c.426C=	NP_001531.1:p.Tyr142=
NM_001540.5:c.426C= MANE Select	NP_001531.1:p.Tyr142=