Canonical Allele Identifier: CA1311924606

Gene: CERKL

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.181558649C= , CM000664.2:g.181558649C=	GRCh38
NC_000002.11:g.182423376C= , CM000664.1:g.182423376C=	GRCh37
NC_000002.10:g.182131621C=	NCBI36
NG_021178.1:g.103459G=
NG_021178.2:g.103459G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684145.1:c.-20G=	ENSP00000508396.1:n.-20G=
ENST00000410087.8:c.737G= MANE Select	ENSP00000386725.3:p.Arg246=
ENST00000339098.9:c.815G=	ENSP00000341159.5:p.Arg272=
ENST00000374967.6:c.673G=	ENSP00000364106.2:n.673G=
ENST00000374969.6:c.482-8941G=	ENSP00000364108.2:n.482-8941G=
ENST00000374970.6:c.614-8941G=	ENSP00000364109.2:n.614-8941G=
ENST00000409440.7:c.683G=	ENSP00000387080.3:p.Arg228=
ENST00000410087.7:c.737G=	ENSP00000386725.3:p.Arg246=
ENST00000421817.5:c.*19G=	ENSP00000411466.1:n.*19G=
ENST00000452174.5:c.541G=	ENSP00000409198.1:n.541G=
ENST00000479558.5:n.735G=
ENST00000494398.5:n.737G=
NM_001030311.2:c.815G=	NP_001025482.1:p.Arg272=
NM_001030312.2:c.482-8941G=	NP_001025483.1:n.482-8941G=
NM_001030313.2:c.614-8941G=	NP_001025484.1:n.614-8941G=
NM_001160277.1:c.683G=	NP_001153749.1:p.Arg228=
NM_201548.4:c.737G=	NP_963842.1:p.Arg246=
NR_027689.1:n.642G=
NR_027690.1:n.774G=
NM_201548.5:c.737G= MANE Select	NP_963842.1:p.Arg246=
NM_001030311.3:c.815G=	NP_001025482.1:p.Arg272=
NM_001030312.3:c.482-8941G=	NP_001025483.1:n.482-8941G=
NM_001030313.3:c.614-8941G=	NP_001025484.1:n.614-8941G=
NM_001160277.2:c.683G=	NP_001153749.1:p.Arg228=
NR_027689.2:n.640G=
NR_027690.2:n.772G=