Canonical Allele Identifier: CA349736710

Gene: CERKL

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.181548679C>T , CM000664.2:g.181548679C>T	GRCh38
NC_000002.11:g.182413406C>T , CM000664.1:g.182413406C>T	GRCh37
NC_000002.10:g.182121651C>T	NCBI36
NG_021178.1:g.113429G>A
NG_021178.2:g.113429G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_201548.5:c.1073+1G>A MANE Select	NP_963842.1:n.1073+1G>A
ENST00000410087.8:c.1073+1G>A MANE Select	ENSP00000386725.3:n.1073+1G>A
NM_001030311.2:c.1151+1G>A	NP_001025482.1:n.1151+1G>A
NM_001030311.3:c.1151+1G>A	NP_001025482.1:n.1151+1G>A
NM_001030312.2:c.734+1G>A	NP_001025483.1:n.734+1G>A
NM_001030312.3:c.734+1G>A	NP_001025483.1:n.734+1G>A
NM_001030313.2:c.866+1G>A	NP_001025484.1:n.866+1G>A
NM_001030313.3:c.866+1G>A	NP_001025484.1:n.866+1G>A
NM_001160277.1:c.1019+1G>A	NP_001153749.1:n.1019+1G>A
NM_001160277.2:c.1019+1G>A	NP_001153749.1:n.1019+1G>A
NM_201548.4:c.1073+1G>A	NP_963842.1:n.1073+1G>A
NR_027689.1:n.978+1G>A
NR_027689.2:n.976+1G>A
NR_027690.1:n.1110+1G>A
NR_027690.2:n.1108+1G>A
ENST00000339098.9:c.1151+1G>A	ENSP00000341159.5:n.1151+1G>A
ENST00000374967.6:c.1009+1G>A	ENSP00000364106.2:n.1009+1G>A
ENST00000374969.6:c.734+1G>A	ENSP00000364108.2:n.734+1G>A
ENST00000374970.6:c.866+1G>A	ENSP00000364109.2:n.866+1G>A
ENST00000409440.7:c.1019+1G>A	ENSP00000387080.3:n.1019+1G>A
ENST00000410087.7:c.1073+1G>A	ENSP00000386725.3:n.1073+1G>A
ENST00000421817.5:c.*355+1G>A	ENSP00000411466.1:n.*355+1G>A
ENST00000452174.5:c.877+1G>A	ENSP00000409198.1:n.877+1G>A
ENST00000479558.5:n.1071+1G>A
ENST00000494398.5:n.1073+1G>A
ENST00000684145.1:c.317+1G>A	ENSP00000508396.1:n.317+1G>A