Canonical Allele Identifier: CA1311924580
Gene: CERKL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.181558585T= , CM000664.2:g.181558585T= GRCh38
NC_000002.11:g.182423312T= , CM000664.1:g.182423312T= GRCh37
NC_000002.10:g.182131557T= NCBI36
NG_021178.1:g.103523A=
NG_021178.2:g.103523A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000684145.1:c.45A= ENSP00000508396.1:p.Pro15=
ENST00000410087.8:c.801A= MANE Select ENSP00000386725.3:p.Pro267=
ENST00000339098.9:c.879A= ENSP00000341159.5:p.Pro293=
ENST00000374967.6:c.737A= ENSP00000364106.2:n.737A=
ENST00000374969.6:c.482-8877A= ENSP00000364108.2:n.482-8877A=
ENST00000374970.6:c.614-8877A= ENSP00000364109.2:n.614-8877A=
ENST00000409440.7:c.747A= ENSP00000387080.3:p.Pro249=
ENST00000410087.7:c.801A= ENSP00000386725.3:p.Pro267=
ENST00000421817.5:c.*83A= ENSP00000411466.1:n.*83A=
ENST00000452174.5:c.605A= ENSP00000409198.1:n.605A=
ENST00000479558.5:n.799A=
ENST00000494398.5:n.801A=
NM_001030311.2:c.879A= NP_001025482.1:p.Pro293=
NM_001030312.2:c.482-8877A= NP_001025483.1:n.482-8877A=
NM_001030313.2:c.614-8877A= NP_001025484.1:n.614-8877A=
NM_001160277.1:c.747A= NP_001153749.1:p.Pro249=
NM_201548.4:c.801A= NP_963842.1:p.Pro267=
NR_027689.1:n.706A=
NR_027690.1:n.838A=
NM_201548.5:c.801A= MANE Select NP_963842.1:p.Pro267=
NM_001030311.3:c.879A= NP_001025482.1:p.Pro293=
NM_001030312.3:c.482-8877A= NP_001025483.1:n.482-8877A=
NM_001030313.3:c.614-8877A= NP_001025484.1:n.614-8877A=
NM_001160277.2:c.747A= NP_001153749.1:p.Pro249=
NR_027689.2:n.704A=
NR_027690.2:n.836A=