Canonical Allele Identifier: CA1718330674

Gene: HSPB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.76303762T= , CM000669.2:g.76303762T=	GRCh38
NC_000007.13:g.75933079T= , CM000669.1:g.75933079T=	GRCh37
NC_000007.12:g.75771015T=	NCBI36
NG_008995.1:g.6205T= , LRG_248:g.6205T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248553.7:c.365-40T= MANE Select	ENSP00000248553.6:n.365-40T=
ENST00000674547.1:c.365-40T=	ENSP00000502461.1:n.365-40T=
ENST00000674638.1:c.365-45T=	ENSP00000502651.1:n.365-45T=
ENST00000674650.1:c.365-222T=	ENSP00000501628.1:n.365-222T=
ENST00000674965.1:c.365-15T=	ENSP00000501765.1:n.365-15T=
ENST00000675134.1:c.365-40T=	ENSP00000501831.1:n.365-40T=
ENST00000675226.1:c.369-45T=	ENSP00000502510.1:n.369-45T=
ENST00000675417.1:n.558T=
ENST00000675538.1:c.400-40T=	ENSP00000502495.1:n.400-40T=
ENST00000675733.1:n.405T=
ENST00000675906.1:c.365-40T=	ENSP00000502714.1:n.365-40T=
ENST00000676195.1:n.81-40T=
ENST00000676231.1:c.394+35T=	ENSP00000502249.1:n.394+35T=
ENST00000248553.6:c.365-40T=	ENSP00000248553.6:n.365-40T=
ENST00000429938.1:c.-141+35T=	ENSP00000405285.1:n.-141+35T=
ENST00000447574.1:c.*489T=	ENSP00000414357.1:n.*489T=
NM_001540.3:c.365-40T= , LRG_248t1:c.365-40T=	NP_001531.1:n.365-40T=
NM_001540.4:c.365-40T=	NP_001531.1:n.365-40T=
NM_001540.5:c.365-40T= MANE Select	NP_001531.1:n.365-40T=