Canonical Allele Identifier: CA1311924599
Gene: CERKL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.181558624T= , CM000664.2:g.181558624T= GRCh38
NC_000002.11:g.182423351T= , CM000664.1:g.182423351T= GRCh37
NC_000002.10:g.182131596T= NCBI36
NG_021178.1:g.103484A=
NG_021178.2:g.103484A=

Transcript Alleles

HGVS Amino-acid change
ENST00000684145.1:c.6A= ENSP00000508396.1:p.Glu2=
ENST00000410087.8:c.762A= MANE Select ENSP00000386725.3:p.Glu254=
ENST00000339098.9:c.840A= ENSP00000341159.5:p.Glu280=
ENST00000374967.6:c.698A= ENSP00000364106.2:n.698A=
ENST00000374969.6:c.482-8916A= ENSP00000364108.2:n.482-8916A=
ENST00000374970.6:c.614-8916A= ENSP00000364109.2:n.614-8916A=
ENST00000409440.7:c.708A= ENSP00000387080.3:p.Glu236=
ENST00000410087.7:c.762A= ENSP00000386725.3:p.Glu254=
ENST00000421817.5:c.*44A= ENSP00000411466.1:n.*44A=
ENST00000452174.5:c.566A= ENSP00000409198.1:n.566A=
ENST00000479558.5:n.760A=
ENST00000494398.5:n.762A=
NM_001030311.2:c.840A= NP_001025482.1:p.Glu280=
NM_001030312.2:c.482-8916A= NP_001025483.1:n.482-8916A=
NM_001030313.2:c.614-8916A= NP_001025484.1:n.614-8916A=
NM_001160277.1:c.708A= NP_001153749.1:p.Glu236=
NM_201548.4:c.762A= NP_963842.1:p.Glu254=
NR_027689.1:n.667A=
NR_027690.1:n.799A=
NM_201548.5:c.762A= MANE Select NP_963842.1:p.Glu254=
NM_001030311.3:c.840A= NP_001025482.1:p.Glu280=
NM_001030312.3:c.482-8916A= NP_001025483.1:n.482-8916A=
NM_001030313.3:c.614-8916A= NP_001025484.1:n.614-8916A=
NM_001160277.2:c.708A= NP_001153749.1:p.Glu236=
NR_027689.2:n.665A=
NR_027690.2:n.797A=