Canonical Allele Identifier: CA367765532

Gene: HSPB1

Linked Data

• MyVariant Identifiers: chr7:g.75933169A>C (hg19) ; chr7:g.76303852A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.76303852A>C , CM000669.2:g.76303852A>C	GRCh38
NC_000007.13:g.75933169A>C , CM000669.1:g.75933169A>C	GRCh37
NC_000007.12:g.75771105A>C	NCBI36
NG_008995.1:g.6295A>C , LRG_248:g.6295A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248553.7:c.415A>C MANE Select	ENSP00000248553.6:p.Thr139Pro
ENST00000674547.1:c.415A>C	ENSP00000502461.1:p.Thr139Pro
ENST00000674638.1:c.410A>C	ENSP00000502651.1:p.His137Pro
ENST00000674650.1:c.365-132A>C	ENSP00000501628.1:n.365-132A>C
ENST00000674965.1:c.*71A>C	ENSP00000501765.1:n.*71A>C
ENST00000675134.1:c.407+8A>C	ENSP00000501831.1:n.407+8A>C
ENST00000675226.1:c.414A>C	ENSP00000502510.1:p.Ser138=
ENST00000675417.1:n.648A>C
ENST00000675538.1:c.450A>C	ENSP00000502495.1:p.Ser150=
ENST00000675906.1:c.415A>C	ENSP00000502714.1:p.Thr139Pro
ENST00000676195.1:n.131A>C
ENST00000676231.1:c.445A>C	ENSP00000502249.1:p.Thr149Pro
ENST00000248553.6:c.415A>C	ENSP00000248553.6:p.Thr139Pro
ENST00000429938.1:c.-90A>C	ENSP00000405285.1:n.-90A>C
ENST00000447574.1:c.*579A>C	ENSP00000414357.1:n.*579A>C
NM_001540.3:c.415A>C , LRG_248t1:c.415A>C	NP_001531.1:p.Thr139Pro
NM_001540.4:c.415A>C	NP_001531.1:p.Thr139Pro
NM_001540.5:c.415A>C MANE Select	NP_001531.1:p.Thr139Pro