Canonical Allele Identifier: CA456330507

Gene: HSPB1

Linked Data

• MyVariant Identifiers: chr7:g.75933156C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.76303839C>A , CM000669.2:g.76303839C>A	GRCh38
NC_000007.13:g.75933156C>A , CM000669.1:g.75933156C>A	GRCh37
NC_000007.12:g.75771092C>A	NCBI36
NG_008995.1:g.6282C>A , LRG_248:g.6282C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248553.7:c.402C>A MANE Select	ENSP00000248553.6:p.Ile134=
ENST00000674547.1:c.402C>A	ENSP00000502461.1:p.Ile134=
ENST00000674638.1:c.397C>A	ENSP00000502651.1:p.Leu133Ile
ENST00000674650.1:c.365-145C>A	ENSP00000501628.1:n.365-145C>A
ENST00000674965.1:c.*58C>A	ENSP00000501765.1:n.*58C>A
ENST00000675134.1:c.402C>A	ENSP00000501831.1:p.Ile134=
ENST00000675226.1:c.401C>A	ENSP00000502510.1:p.Ser134Tyr
ENST00000675417.1:n.635C>A
ENST00000675538.1:c.437C>A	ENSP00000502495.1:p.Ser146Tyr
ENST00000675906.1:c.402C>A	ENSP00000502714.1:p.Ile134=
ENST00000676195.1:n.118C>A
ENST00000676231.1:c.432C>A	ENSP00000502249.1:p.Ile144=
ENST00000248553.6:c.402C>A	ENSP00000248553.6:p.Ile134=
ENST00000429938.1:c.-103C>A	ENSP00000405285.1:n.-103C>A
ENST00000447574.1:c.*566C>A	ENSP00000414357.1:n.*566C>A
NM_001540.3:c.402C>A , LRG_248t1:c.402C>A	NP_001531.1:p.Ile134=
NM_001540.4:c.402C>A	NP_001531.1:p.Ile134=
NM_001540.5:c.402C>A MANE Select	NP_001531.1:p.Ile134=