Canonical Allele Identifier: CA367765546

Gene: HSPB1

Linked Data

• MyVariant Identifiers: chr7:g.75933172C>T (hg19) ; chr7:g.76303855C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.76303855C>T , CM000669.2:g.76303855C>T	GRCh38
NC_000007.13:g.75933172C>T , CM000669.1:g.75933172C>T	GRCh37
NC_000007.12:g.75771108C>T	NCBI36
NG_008995.1:g.6298C>T , LRG_248:g.6298C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248553.7:c.418C>T MANE Select	ENSP00000248553.6:p.Arg140Trp
ENST00000674547.1:c.418C>T	ENSP00000502461.1:p.Arg140Trp
ENST00000674638.1:c.413C>T	ENSP00000502651.1:p.Ala138Val
ENST00000674650.1:c.365-129C>T	ENSP00000501628.1:n.365-129C>T
ENST00000674965.1:c.*74C>T	ENSP00000501765.1:n.*74C>T
ENST00000675134.1:c.407+11C>T	ENSP00000501831.1:n.407+11C>T
ENST00000675226.1:c.417C>T	ENSP00000502510.1:p.Arg139=
ENST00000675417.1:n.651C>T
ENST00000675538.1:c.453C>T	ENSP00000502495.1:p.Arg151=
ENST00000675906.1:c.418C>T	ENSP00000502714.1:p.Arg140Trp
ENST00000676195.1:n.134C>T
ENST00000676231.1:c.448C>T	ENSP00000502249.1:p.Arg150Trp
ENST00000248553.6:c.418C>T	ENSP00000248553.6:p.Arg140Trp
ENST00000429938.1:c.-87C>T	ENSP00000405285.1:n.-87C>T
ENST00000447574.1:c.*582C>T	ENSP00000414357.1:n.*582C>T
NM_001540.3:c.418C>T , LRG_248t1:c.418C>T	NP_001531.1:p.Arg140Trp
NM_001540.4:c.418C>T	NP_001531.1:p.Arg140Trp
NM_001540.5:c.418C>T MANE Select	NP_001531.1:p.Arg140Trp