Canonical Allele Identifier: CA1718330864

Gene: HSPB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.76303821G= , CM000669.2:g.76303821G=	GRCh38
NC_000007.13:g.75933138G= , CM000669.1:g.75933138G=	GRCh37
NC_000007.12:g.75771074G=	NCBI36
NG_008995.1:g.6264G= , LRG_248:g.6264G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248553.7:c.384G= MANE Select	ENSP00000248553.6:p.Gln128=
ENST00000674547.1:c.384G=	ENSP00000502461.1:p.Gln128=
ENST00000674638.1:c.379G=	ENSP00000502651.1:p.Gly127=
ENST00000674650.1:c.365-163G=	ENSP00000501628.1:n.365-163G=
ENST00000674965.1:c.*40G=	ENSP00000501765.1:n.*40G=
ENST00000675134.1:c.384G=	ENSP00000501831.1:p.Gln128=
ENST00000675226.1:c.383G=	ENSP00000502510.1:p.Arg128=
ENST00000675417.1:n.617G=
ENST00000675538.1:c.419G=	ENSP00000502495.1:p.Arg140=
ENST00000675906.1:c.384G=	ENSP00000502714.1:p.Gln128=
ENST00000676195.1:n.100G=
ENST00000676231.1:c.414G=	ENSP00000502249.1:p.Gln138=
ENST00000248553.6:c.384G=	ENSP00000248553.6:p.Gln128=
ENST00000429938.1:c.-121G=	ENSP00000405285.1:n.-121G=
ENST00000447574.1:c.*548G=	ENSP00000414357.1:n.*548G=
NM_001540.3:c.384G= , LRG_248t1:c.384G=	NP_001531.1:p.Gln128=
NM_001540.4:c.384G=	NP_001531.1:p.Gln128=
NM_001540.5:c.384G= MANE Select	NP_001531.1:p.Gln128=