Canonical Allele Identifier: CA1718330877

Gene: HSPB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.76303831G= , CM000669.2:g.76303831G=	GRCh38
NC_000007.13:g.75933148G= , CM000669.1:g.75933148G=	GRCh37
NC_000007.12:g.75771084G=	NCBI36
NG_008995.1:g.6274G= , LRG_248:g.6274G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248553.7:c.394G= MANE Select	ENSP00000248553.6:p.Gly132=
ENST00000674547.1:c.394G=	ENSP00000502461.1:p.Gly132=
ENST00000674638.1:c.389G=	ENSP00000502651.1:p.Trp130=
ENST00000674650.1:c.365-153G=	ENSP00000501628.1:n.365-153G=
ENST00000674965.1:c.*50G=	ENSP00000501765.1:n.*50G=
ENST00000675134.1:c.394G=	ENSP00000501831.1:p.Gly132=
ENST00000675226.1:c.393G=	ENSP00000502510.1:p.Met131=
ENST00000675417.1:n.627G=
ENST00000675538.1:c.429G=	ENSP00000502495.1:p.Met143=
ENST00000675906.1:c.394G=	ENSP00000502714.1:p.Gly132=
ENST00000676195.1:n.110G=
ENST00000676231.1:c.424G=	ENSP00000502249.1:p.Gly142=
ENST00000248553.6:c.394G=	ENSP00000248553.6:p.Gly132=
ENST00000429938.1:c.-111G=	ENSP00000405285.1:n.-111G=
ENST00000447574.1:c.*558G=	ENSP00000414357.1:n.*558G=
NM_001540.3:c.394G= , LRG_248t1:c.394G=	NP_001531.1:p.Gly132=
NM_001540.4:c.394G=	NP_001531.1:p.Gly132=
NM_001540.5:c.394G= MANE Select	NP_001531.1:p.Gly132=