Canonical Allele Identifier: CA456330438

Gene: HSPB1

Linked Data

• MyVariant Identifiers: chr7:g.75933120C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.76303803C>A , CM000669.2:g.76303803C>A	GRCh38
NC_000007.13:g.75933120C>A , CM000669.1:g.75933120C>A	GRCh37
NC_000007.12:g.75771056C>A	NCBI36
NG_008995.1:g.6246C>A , LRG_248:g.6246C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248553.7:c.366C>A MANE Select	ENSP00000248553.6:p.Gly122=
ENST00000674547.1:c.366C>A	ENSP00000502461.1:p.Gly122=
ENST00000674638.1:c.365-4C>A	ENSP00000502651.1:n.365-4C>A
ENST00000674650.1:c.365-181C>A	ENSP00000501628.1:n.365-181C>A
ENST00000674965.1:c.*22C>A	ENSP00000501765.1:n.*22C>A
ENST00000675134.1:c.366C>A	ENSP00000501831.1:p.Gly122=
ENST00000675226.1:c.369-4C>A	ENSP00000502510.1:n.369-4C>A
ENST00000675417.1:n.599C>A
ENST00000675538.1:c.401C>A	ENSP00000502495.1:p.Ala134Glu
ENST00000675906.1:c.366C>A	ENSP00000502714.1:p.Gly122=
ENST00000676195.1:n.82C>A
ENST00000676231.1:c.396C>A	ENSP00000502249.1:p.Gly132=
ENST00000248553.6:c.366C>A	ENSP00000248553.6:p.Gly122=
ENST00000429938.1:c.-139C>A	ENSP00000405285.1:n.-139C>A
ENST00000447574.1:c.*530C>A	ENSP00000414357.1:n.*530C>A
NM_001540.3:c.366C>A , LRG_248t1:c.366C>A	NP_001531.1:p.Gly122=
NM_001540.4:c.366C>A	NP_001531.1:p.Gly122=
NM_001540.5:c.366C>A MANE Select	NP_001531.1:p.Gly122=