Canonical Allele Identifier: CA1718331351

Gene: HSPB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.76304007C= , CM000669.2:g.76304007C=	GRCh38
NC_000007.13:g.75933324C= , CM000669.1:g.75933324C=	GRCh37
NC_000007.12:g.75771260C=	NCBI36
NG_008995.1:g.6450C= , LRG_248:g.6450C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001540.5:c.452C= MANE Select	NP_001531.1:p.Thr151=
ENST00000248553.7:c.452C= MANE Select	ENSP00000248553.6:p.Thr151=
NM_001540.3:c.452C= , LRG_248t1:c.452C=	NP_001531.1:p.Thr151=
NM_001540.4:c.452C=	NP_001531.1:p.Thr151=
ENST00000248553.6:c.452C=	ENSP00000248553.6:p.Thr151=
ENST00000429938.1:c.-53C=	ENSP00000405285.1:n.-53C=
ENST00000447574.1:c.*616C=	ENSP00000414357.1:n.*616C=
ENST00000674547.1:c.*43C=	ENSP00000502461.1:n.*43C=
ENST00000674638.1:c.447C=	ENSP00000502651.1:p.His149=
ENST00000674650.1:c.388C=	ENSP00000501628.1:p.Pro130=
ENST00000674965.1:c.*108C=	ENSP00000501765.1:n.*108C=
ENST00000675134.1:c.431C=	ENSP00000501831.1:p.Thr144=
ENST00000675226.1:c.451C=	ENSP00000502510.1:p.Pro151=
ENST00000675417.1:n.803C=
ENST00000675538.1:c.487C=	ENSP00000502495.1:p.Pro163=
ENST00000675906.1:c.*37C=	ENSP00000502714.1:n.*37C=
ENST00000676231.1:c.482C=	ENSP00000502249.1:p.Thr161=