Canonical Allele Identifier: CA1718330835

Gene: HSPB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.76303816C= , CM000669.2:g.76303816C=	GRCh38
NC_000007.13:g.75933133C= , CM000669.1:g.75933133C=	GRCh37
NC_000007.12:g.75771069C=	NCBI36
NG_008995.1:g.6259C= , LRG_248:g.6259C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248553.7:c.379C= MANE Select	ENSP00000248553.6:p.Arg127=
ENST00000674547.1:c.379C=	ENSP00000502461.1:p.Arg127=
ENST00000674638.1:c.374C=	ENSP00000502651.1:p.Ala125=
ENST00000674650.1:c.365-168C=	ENSP00000501628.1:n.365-168C=
ENST00000674965.1:c.*35C=	ENSP00000501765.1:n.*35C=
ENST00000675134.1:c.379C=	ENSP00000501831.1:p.Arg127=
ENST00000675226.1:c.378C=	ENSP00000502510.1:p.Ser126=
ENST00000675417.1:n.612C=
ENST00000675538.1:c.414C=	ENSP00000502495.1:p.Ser138=
ENST00000675906.1:c.379C=	ENSP00000502714.1:p.Arg127=
ENST00000676195.1:n.95C=
ENST00000676231.1:c.409C=	ENSP00000502249.1:p.Arg137=
ENST00000248553.6:c.379C=	ENSP00000248553.6:p.Arg127=
ENST00000429938.1:c.-126C=	ENSP00000405285.1:n.-126C=
ENST00000447574.1:c.*543C=	ENSP00000414357.1:n.*543C=
NM_001540.3:c.379C= , LRG_248t1:c.379C=	NP_001531.1:p.Arg127=
NM_001540.4:c.379C=	NP_001531.1:p.Arg127=
NM_001540.5:c.379C= MANE Select	NP_001531.1:p.Arg127=