Canonical Allele Identifier: CA349741156

Gene: CERKL

Linked Data

• MyVariant Identifiers: chr2:g.182423435A>T (hg19) ; chr2:g.181558708A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.181558708A>T , CM000664.2:g.181558708A>T	GRCh38
NC_000002.11:g.182423435A>T , CM000664.1:g.182423435A>T	GRCh37
NC_000002.10:g.182131680A>T	NCBI36
NG_021178.1:g.103400T>A
NG_021178.2:g.103400T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684145.1:c.-79T>A	ENSP00000508396.1:n.-79T>A
ENST00000410087.8:c.678T>A MANE Select	ENSP00000386725.3:p.Gly226=
ENST00000339098.9:c.756T>A	ENSP00000341159.5:p.Ser252Arg
ENST00000374967.6:c.614T>A	ENSP00000364106.2:p.Met205Lys
ENST00000374969.6:c.482-9000T>A	ENSP00000364108.2:n.482-9000T>A
ENST00000374970.6:c.614-9000T>A	ENSP00000364109.2:n.614-9000T>A
ENST00000409440.7:c.624T>A	ENSP00000387080.3:p.Ser208Arg
ENST00000410087.7:c.678T>A	ENSP00000386725.3:p.Gly226=
ENST00000421817.5:c.482T>A	ENSP00000411466.1:p.Val161Glu
ENST00000452174.5:c.482T>A	ENSP00000409198.1:p.Val161Glu
ENST00000466715.5:n.494T>A
ENST00000479558.5:n.676T>A
ENST00000494398.5:n.678T>A
NM_001030311.2:c.756T>A	NP_001025482.1:p.Ser252Arg
NM_001030312.2:c.482-9000T>A	NP_001025483.1:n.482-9000T>A
NM_001030313.2:c.614-9000T>A	NP_001025484.1:n.614-9000T>A
NM_001160277.1:c.624T>A	NP_001153749.1:p.Ser208Arg
NM_201548.4:c.678T>A	NP_963842.1:p.Gly226=
NR_027689.1:n.583T>A
NR_027690.1:n.715T>A
NM_201548.5:c.678T>A MANE Select	NP_963842.1:p.Gly226=
NM_001030311.3:c.756T>A	NP_001025482.1:p.Ser252Arg
NM_001030312.3:c.482-9000T>A	NP_001025483.1:n.482-9000T>A
NM_001030313.3:c.614-9000T>A	NP_001025484.1:n.614-9000T>A
NM_001160277.2:c.624T>A	NP_001153749.1:p.Ser208Arg
NR_027689.2:n.581T>A
NR_027690.2:n.713T>A