Canonical Allele Identifier: CA2010465

Gene: CERKL

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.181544750G>A , CM000664.2:g.181544750G>A	GRCh38
NC_000002.11:g.182409477G>A , CM000664.1:g.182409477G>A	GRCh37
NC_000002.10:g.182117722G>A	NCBI36
NG_021178.1:g.117358C>T
NG_021178.2:g.117358C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684145.1:c.559C>T	ENSP00000508396.1:p.Arg187Trp
ENST00000410087.8:c.1315C>T MANE Select	ENSP00000386725.3:p.Arg439Trp
ENST00000339098.9:c.1393C>T	ENSP00000341159.5:p.Arg465Trp
ENST00000374967.6:c.1251C>T	ENSP00000364106.2:n.1251C>T
ENST00000374969.6:c.976C>T	ENSP00000364108.2:p.Arg326Trp
ENST00000374970.6:c.1108C>T	ENSP00000364109.2:p.Arg370Trp
ENST00000409440.7:c.1261C>T	ENSP00000387080.3:p.Arg421Trp
ENST00000410087.7:c.1315C>T	ENSP00000386725.3:p.Arg439Trp
ENST00000421817.5:c.*571C>T	ENSP00000411466.1:n.*571C>T
ENST00000452174.5:c.1119C>T	ENSP00000409198.1:n.1119C>T
ENST00000479558.5:n.1313C>T
ENST00000494398.5:n.2107C>T
NM_001030311.2:c.1393C>T	NP_001025482.1:p.Arg465Trp
NM_001030312.2:c.976C>T	NP_001025483.1:p.Arg326Trp
NM_001030313.2:c.1108C>T	NP_001025484.1:p.Arg370Trp
NM_001160277.1:c.1261C>T	NP_001153749.1:p.Arg421Trp
NM_201548.4:c.1315C>T	NP_963842.1:p.Arg439Trp
NR_027689.1:n.1220C>T
NR_027690.1:n.1352C>T
NM_201548.5:c.1315C>T MANE Select	NP_963842.1:p.Arg439Trp
NM_001030311.3:c.1393C>T	NP_001025482.1:p.Arg465Trp
NM_001030312.3:c.976C>T	NP_001025483.1:p.Arg326Trp
NM_001030313.3:c.1108C>T	NP_001025484.1:p.Arg370Trp
NM_001160277.2:c.1261C>T	NP_001153749.1:p.Arg421Trp
NR_027689.2:n.1218C>T
NR_027690.2:n.1350C>T