Canonical Allele Identifier: CA456330424

Gene: HSPB1

Linked Data

• MyVariant Identifiers: chr7:g.75933174G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.76303857G>T , CM000669.2:g.76303857G>T	GRCh38
NC_000007.13:g.75933174G>T , CM000669.1:g.75933174G>T	GRCh37
NC_000007.12:g.75771110G>T	NCBI36
NG_008995.1:g.6300G>T , LRG_248:g.6300G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000248553.7:c.420G>T MANE Select	ENSP00000248553.6:p.Arg140=
ENST00000674547.1:c.420G>T	ENSP00000502461.1:p.Arg140=
ENST00000674638.1:c.415G>T	ENSP00000502651.1:p.Glu139Ter
ENST00000674650.1:c.365-127G>T	ENSP00000501628.1:n.365-127G>T
ENST00000674965.1:c.*76G>T	ENSP00000501765.1:n.*76G>T
ENST00000675134.1:c.407+13G>T	ENSP00000501831.1:n.407+13G>T
ENST00000675226.1:c.419G>T	ENSP00000502510.1:p.Gly140Val
ENST00000675417.1:n.653G>T
ENST00000675538.1:c.455G>T	ENSP00000502495.1:p.Gly152Val
ENST00000675906.1:c.420G>T	ENSP00000502714.1:p.Arg140=
ENST00000676195.1:n.136G>T
ENST00000676231.1:c.450G>T	ENSP00000502249.1:p.Arg150=
ENST00000248553.6:c.420G>T	ENSP00000248553.6:p.Arg140=
ENST00000429938.1:c.-85G>T	ENSP00000405285.1:n.-85G>T
ENST00000447574.1:c.*584G>T	ENSP00000414357.1:n.*584G>T
NM_001540.3:c.420G>T , LRG_248t1:c.420G>T	NP_001531.1:p.Arg140=
NM_001540.4:c.420G>T	NP_001531.1:p.Arg140=
NM_001540.5:c.420G>T MANE Select	NP_001531.1:p.Arg140=