Canonical Allele Identifier: CA1311924595

Gene: CERKL

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.181558617G= , CM000664.2:g.181558617G=	GRCh38
NC_000002.11:g.182423344G= , CM000664.1:g.182423344G=	GRCh37
NC_000002.10:g.182131589G=	NCBI36
NG_021178.1:g.103491C=
NG_021178.2:g.103491C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684145.1:c.13C=	ENSP00000508396.1:p.Arg5=
ENST00000410087.8:c.769C= MANE Select	ENSP00000386725.3:p.Arg257=
ENST00000339098.9:c.847C=	ENSP00000341159.5:p.Arg283=
ENST00000374967.6:c.705C=	ENSP00000364106.2:n.705C=
ENST00000374969.6:c.482-8909C=	ENSP00000364108.2:n.482-8909C=
ENST00000374970.6:c.614-8909C=	ENSP00000364109.2:n.614-8909C=
ENST00000409440.7:c.715C=	ENSP00000387080.3:p.Arg239=
ENST00000410087.7:c.769C=	ENSP00000386725.3:p.Arg257=
ENST00000421817.5:c.*51C=	ENSP00000411466.1:n.*51C=
ENST00000452174.5:c.573C=	ENSP00000409198.1:n.573C=
ENST00000479558.5:n.767C=
ENST00000494398.5:n.769C=
NM_001030311.2:c.847C=	NP_001025482.1:p.Arg283=
NM_001030312.2:c.482-8909C=	NP_001025483.1:n.482-8909C=
NM_001030313.2:c.614-8909C=	NP_001025484.1:n.614-8909C=
NM_001160277.1:c.715C=	NP_001153749.1:p.Arg239=
NM_201548.4:c.769C=	NP_963842.1:p.Arg257=
NR_027689.1:n.674C=
NR_027690.1:n.806C=
NM_201548.5:c.769C= MANE Select	NP_963842.1:p.Arg257=
NM_001030311.3:c.847C=	NP_001025482.1:p.Arg283=
NM_001030312.3:c.482-8909C=	NP_001025483.1:n.482-8909C=
NM_001030313.3:c.614-8909C=	NP_001025484.1:n.614-8909C=
NM_001160277.2:c.715C=	NP_001153749.1:p.Arg239=
NR_027689.2:n.672C=
NR_027690.2:n.804C=