Canonical Allele Identifier: CA1718330874

Gene: HSPB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.76303830T= , CM000669.2:g.76303830T=	GRCh38
NC_000007.13:g.75933147T= , CM000669.1:g.75933147T=	GRCh37
NC_000007.12:g.75771083T=	NCBI36
NG_008995.1:g.6273T= , LRG_248:g.6273T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248553.7:c.393T= MANE Select	ENSP00000248553.6:p.His131=
ENST00000674547.1:c.393T=	ENSP00000502461.1:p.His131=
ENST00000674638.1:c.388T=	ENSP00000502651.1:p.Trp130=
ENST00000674650.1:c.365-154T=	ENSP00000501628.1:n.365-154T=
ENST00000674965.1:c.*49T=	ENSP00000501765.1:n.*49T=
ENST00000675134.1:c.393T=	ENSP00000501831.1:p.His131=
ENST00000675226.1:c.392T=	ENSP00000502510.1:p.Met131=
ENST00000675417.1:n.626T=
ENST00000675538.1:c.428T=	ENSP00000502495.1:p.Met143=
ENST00000675906.1:c.393T=	ENSP00000502714.1:p.His131=
ENST00000676195.1:n.109T=
ENST00000676231.1:c.423T=	ENSP00000502249.1:p.His141=
ENST00000248553.6:c.393T=	ENSP00000248553.6:p.His131=
ENST00000429938.1:c.-112T=	ENSP00000405285.1:n.-112T=
ENST00000447574.1:c.*557T=	ENSP00000414357.1:n.*557T=
NM_001540.3:c.393T= , LRG_248t1:c.393T=	NP_001531.1:p.His131=
NM_001540.4:c.393T=	NP_001531.1:p.His131=
NM_001540.5:c.393T= MANE Select	NP_001531.1:p.His131=