Canonical Allele Identifier: CA1718330884

Gene: HSPB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.76303839C= , CM000669.2:g.76303839C=	GRCh38
NC_000007.13:g.75933156C= , CM000669.1:g.75933156C=	GRCh37
NC_000007.12:g.75771092C=	NCBI36
NG_008995.1:g.6282C= , LRG_248:g.6282C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248553.7:c.402C= MANE Select	ENSP00000248553.6:p.Ile134=
ENST00000674547.1:c.402C=	ENSP00000502461.1:p.Ile134=
ENST00000674638.1:c.397C=	ENSP00000502651.1:p.Leu133=
ENST00000674650.1:c.365-145C=	ENSP00000501628.1:n.365-145C=
ENST00000674965.1:c.*58C=	ENSP00000501765.1:n.*58C=
ENST00000675134.1:c.402C=	ENSP00000501831.1:p.Ile134=
ENST00000675226.1:c.401C=	ENSP00000502510.1:p.Ser134=
ENST00000675417.1:n.635C=
ENST00000675538.1:c.437C=	ENSP00000502495.1:p.Ser146=
ENST00000675906.1:c.402C=	ENSP00000502714.1:p.Ile134=
ENST00000676195.1:n.118C=
ENST00000676231.1:c.432C=	ENSP00000502249.1:p.Ile144=
ENST00000248553.6:c.402C=	ENSP00000248553.6:p.Ile134=
ENST00000429938.1:c.-103C=	ENSP00000405285.1:n.-103C=
ENST00000447574.1:c.*566C=	ENSP00000414357.1:n.*566C=
NM_001540.3:c.402C= , LRG_248t1:c.402C=	NP_001531.1:p.Ile134=
NM_001540.4:c.402C=	NP_001531.1:p.Ile134=
NM_001540.5:c.402C= MANE Select	NP_001531.1:p.Ile134=