Canonical Allele Identifier: CA2543604217
Gene: CERKL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.181558684_181558690del , CM000664.2:g.181558684_181558690del GRCh38
NC_000002.11:g.182423411_182423417del , CM000664.1:g.182423411_182423417del GRCh37
NC_000002.10:g.182131656_182131662del NCBI36
NG_021178.1:g.103418_103424del
NG_021178.2:g.103418_103424del

Transcript Alleles

HGVS Amino-acid Change
ENST00000684145.1:c.-61_-55del ENSP00000508396.1:n.-61_-55del
ENST00000410087.8:c.696_702del MANE Select ENSP00000386725.3:p.Asp233LeufsTer5
ENST00000339098.9:c.774_780del ENSP00000341159.5:p.Asp259LeufsTer5
ENST00000374967.6:c.632_638del ENSP00000364106.2:p.Glu211ValfsTer3
ENST00000374969.6:c.482-8982_482-8976del ENSP00000364108.2:n.482-8982_482-8976del
ENST00000374970.6:c.614-8982_614-8976del ENSP00000364109.2:n.614-8982_614-8976del
ENST00000409440.7:c.642_648del ENSP00000387080.3:p.Asp215LeufsTer5
ENST00000410087.7:c.696_702del ENSP00000386725.3:p.Asp233LeufsTer5
ENST00000421817.5:c.500_506del ENSP00000411466.1:p.Glu167ValfsTer3
ENST00000452174.5:c.500_506del ENSP00000409198.1:p.Glu167ValfsTer3
ENST00000466715.5:n.512_518del
ENST00000479558.5:n.694_700del
ENST00000494398.5:n.696_702del
NM_001030311.2:c.774_780del NP_001025482.1:p.Asp259LeufsTer5
NM_001030312.2:c.482-8982_482-8976del NP_001025483.1:n.482-8982_482-8976del
NM_001030313.2:c.614-8982_614-8976del NP_001025484.1:n.614-8982_614-8976del
NM_001160277.1:c.642_648del NP_001153749.1:p.Asp215LeufsTer5
NM_201548.4:c.696_702del NP_963842.1:p.Asp233LeufsTer5
NR_027689.1:n.601_607del
NR_027690.1:n.733_739del
NM_201548.5:c.696_702del MANE Select NP_963842.1:p.Asp233LeufsTer5
NM_001030311.3:c.774_780del NP_001025482.1:p.Asp259LeufsTer5
NM_001030312.3:c.482-8982_482-8976del NP_001025483.1:n.482-8982_482-8976del
NM_001030313.3:c.614-8982_614-8976del NP_001025484.1:n.614-8982_614-8976del
NM_001160277.2:c.642_648del NP_001153749.1:p.Asp215LeufsTer5
NR_027689.2:n.599_605del
NR_027690.2:n.731_737del