Canonical Allele Identifier: CA2578916980

Gene: HSPB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.76303902dup , CM000669.2:g.76303902dup	GRCh38
NC_000007.13:g.75933219dup , CM000669.1:g.75933219dup	GRCh37
NC_000007.12:g.75771155dup	NCBI36
NG_008995.1:g.6345dup , LRG_248:g.6345dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248553.7:c.428+37dup MANE Select	ENSP00000248553.6:n.428+37dup
ENST00000674547.1:c.*19+14dup	ENSP00000502461.1:n.*19+14dup
ENST00000674638.1:c.423+37dup	ENSP00000502651.1:n.423+37dup
ENST00000674650.1:c.365-82dup	ENSP00000501628.1:n.365-82dup
ENST00000674965.1:c.*84+37dup	ENSP00000501765.1:n.*84+37dup
ENST00000675134.1:c.407+58dup	ENSP00000501831.1:n.407+58dup
ENST00000675226.1:c.427+37dup	ENSP00000502510.1:n.427+37dup
ENST00000675417.1:n.698dup
ENST00000675538.1:c.463+37dup	ENSP00000502495.1:n.463+37dup
ENST00000675906.1:c.*13+20dup	ENSP00000502714.1:n.*13+20dup
ENST00000676231.1:c.458+37dup	ENSP00000502249.1:n.458+37dup
ENST00000248553.6:c.428+37dup	ENSP00000248553.6:n.428+37dup
ENST00000429938.1:c.-77+37dup	ENSP00000405285.1:n.-77+37dup
ENST00000447574.1:c.*592+37dup	ENSP00000414357.1:n.*592+37dup
NM_001540.3:c.428+37dup , LRG_248t1:c.428+37dup	NP_001531.1:n.428+37dup
NM_001540.4:c.428+37dup	NP_001531.1:n.428+37dup
NM_001540.5:c.428+37dup MANE Select	NP_001531.1:n.428+37dup