Canonical Allele Identifier: CA367765608

Gene: HSPB1

Linked Data

• gnomAD v4: 7-76303866-G-T
• MyVariant Identifiers: chr7:g.75933183G>T (hg19) ; chr7:g.76303866G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.76303866G>T , CM000669.2:g.76303866G>T	GRCh38
NC_000007.13:g.75933183G>T , CM000669.1:g.75933183G>T	GRCh37
NC_000007.12:g.75771119G>T	NCBI36
NG_008995.1:g.6309G>T , LRG_248:g.6309G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000248553.7:c.428+1G>T MANE Select	ENSP00000248553.6:n.428+1G>T
ENST00000674547.1:c.429G>T	ENSP00000502461.1:p.Thr143=
ENST00000674638.1:c.423+1G>T	ENSP00000502651.1:n.423+1G>T
ENST00000674650.1:c.365-118G>T	ENSP00000501628.1:n.365-118G>T
ENST00000674965.1:c.*84+1G>T	ENSP00000501765.1:n.*84+1G>T
ENST00000675134.1:c.407+22G>T	ENSP00000501831.1:n.407+22G>T
ENST00000675226.1:c.427+1G>T	ENSP00000502510.1:n.427+1G>T
ENST00000675417.1:n.662G>T
ENST00000675538.1:c.463+1G>T	ENSP00000502495.1:n.463+1G>T
ENST00000675906.1:c.429G>T	ENSP00000502714.1:p.Thr143=
ENST00000676231.1:c.458+1G>T	ENSP00000502249.1:n.458+1G>T
ENST00000248553.6:c.428+1G>T	ENSP00000248553.6:n.428+1G>T
ENST00000429938.1:c.-77+1G>T	ENSP00000405285.1:n.-77+1G>T
ENST00000447574.1:c.*592+1G>T	ENSP00000414357.1:n.*592+1G>T
NM_001540.3:c.428+1G>T , LRG_248t1:c.428+1G>T	NP_001531.1:n.428+1G>T
NM_001540.4:c.428+1G>T	NP_001531.1:n.428+1G>T
NM_001540.5:c.428+1G>T MANE Select	NP_001531.1:n.428+1G>T