Canonical Allele Identifier: CA1311924673
Gene: CERKL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.181558799T= , CM000664.2:g.181558799T= GRCh38
NC_000002.11:g.182423526T= , CM000664.1:g.182423526T= GRCh37
NC_000002.10:g.182131771T= NCBI36
NG_021178.1:g.103309A=
NG_021178.2:g.103309A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000684145.1:c.-79-91A= ENSP00000508396.1:n.-79-91A=
ENST00000410087.8:c.678-91A= MANE Select ENSP00000386725.3:n.678-91A=
ENST00000339098.9:c.756-91A= ENSP00000341159.5:n.756-91A=
ENST00000374967.6:c.614-91A= ENSP00000364106.2:n.614-91A=
ENST00000374969.6:c.482-9091A= ENSP00000364108.2:n.482-9091A=
ENST00000374970.6:c.614-9091A= ENSP00000364109.2:n.614-9091A=
ENST00000409440.7:c.624-91A= ENSP00000387080.3:n.624-91A=
ENST00000410087.7:c.678-91A= ENSP00000386725.3:n.678-91A=
ENST00000421817.5:c.482-91A= ENSP00000411466.1:n.482-91A=
ENST00000452174.5:c.482-91A= ENSP00000409198.1:n.482-91A=
ENST00000466715.5:n.494-91A=
ENST00000479558.5:n.676-91A=
ENST00000494398.5:n.678-91A=
NM_001030311.2:c.756-91A= NP_001025482.1:n.756-91A=
NM_001030312.2:c.482-9091A= NP_001025483.1:n.482-9091A=
NM_001030313.2:c.614-9091A= NP_001025484.1:n.614-9091A=
NM_001160277.1:c.624-91A= NP_001153749.1:n.624-91A=
NM_201548.4:c.678-91A= NP_963842.1:n.678-91A=
NR_027689.1:n.583-91A=
NR_027690.1:n.715-91A=
NM_201548.5:c.678-91A= MANE Select NP_963842.1:n.678-91A=
NM_001030311.3:c.756-91A= NP_001025482.1:n.756-91A=
NM_001030312.3:c.482-9091A= NP_001025483.1:n.482-9091A=
NM_001030313.3:c.614-9091A= NP_001025484.1:n.614-9091A=
NM_001160277.2:c.624-91A= NP_001153749.1:n.624-91A=
NR_027689.2:n.581-91A=
NR_027690.2:n.713-91A=