Canonical Allele Identifier: CA1311924608
Gene: CERKL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.181558652A= , CM000664.2:g.181558652A= GRCh38
NC_000002.11:g.182423379A= , CM000664.1:g.182423379A= GRCh37
NC_000002.10:g.182131624A= NCBI36
NG_021178.1:g.103456T=
NG_021178.2:g.103456T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000684145.1:c.-23T= ENSP00000508396.1:n.-23T=
ENST00000410087.8:c.734T= MANE Select ENSP00000386725.3:p.Leu245=
ENST00000339098.9:c.812T= ENSP00000341159.5:p.Leu271=
ENST00000374967.6:c.670T= ENSP00000364106.2:n.670T=
ENST00000374969.6:c.482-8944T= ENSP00000364108.2:n.482-8944T=
ENST00000374970.6:c.614-8944T= ENSP00000364109.2:n.614-8944T=
ENST00000409440.7:c.680T= ENSP00000387080.3:p.Leu227=
ENST00000410087.7:c.734T= ENSP00000386725.3:p.Leu245=
ENST00000421817.5:c.*16T= ENSP00000411466.1:n.*16T=
ENST00000452174.5:c.538T= ENSP00000409198.1:n.538T=
ENST00000466715.5:n.550T=
ENST00000479558.5:n.732T=
ENST00000494398.5:n.734T=
NM_001030311.2:c.812T= NP_001025482.1:p.Leu271=
NM_001030312.2:c.482-8944T= NP_001025483.1:n.482-8944T=
NM_001030313.2:c.614-8944T= NP_001025484.1:n.614-8944T=
NM_001160277.1:c.680T= NP_001153749.1:p.Leu227=
NM_201548.4:c.734T= NP_963842.1:p.Leu245=
NR_027689.1:n.639T=
NR_027690.1:n.771T=
NM_201548.5:c.734T= MANE Select NP_963842.1:p.Leu245=
NM_001030311.3:c.812T= NP_001025482.1:p.Leu271=
NM_001030312.3:c.482-8944T= NP_001025483.1:n.482-8944T=
NM_001030313.3:c.614-8944T= NP_001025484.1:n.614-8944T=
NM_001160277.2:c.680T= NP_001153749.1:p.Leu227=
NR_027689.2:n.637T=
NR_027690.2:n.769T=