Canonical Allele Identifier: CA349737616

Gene: CERKL

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.181549633C>T , CM000664.2:g.181549633C>T	GRCh38
NC_000002.11:g.182414360C>T , CM000664.1:g.182414360C>T	GRCh37
NC_000002.10:g.182122605C>T	NCBI36
NG_021178.1:g.112475G>A
NG_021178.2:g.112475G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_201548.5:c.895+1G>A MANE Select	NP_963842.1:n.895+1G>A
ENST00000410087.8:c.895+1G>A MANE Select	ENSP00000386725.3:n.895+1G>A
NM_001030311.2:c.973+1G>A	NP_001025482.1:n.973+1G>A
NM_001030311.3:c.973+1G>A	NP_001025482.1:n.973+1G>A
NM_001030312.2:c.556+1G>A	NP_001025483.1:n.556+1G>A
NM_001030312.3:c.556+1G>A	NP_001025483.1:n.556+1G>A
NM_001030313.2:c.688+1G>A	NP_001025484.1:n.688+1G>A
NM_001030313.3:c.688+1G>A	NP_001025484.1:n.688+1G>A
NM_001160277.1:c.841+1G>A	NP_001153749.1:n.841+1G>A
NM_001160277.2:c.841+1G>A	NP_001153749.1:n.841+1G>A
NM_201548.4:c.895+1G>A	NP_963842.1:n.895+1G>A
NR_027689.1:n.800+1G>A
NR_027689.2:n.798+1G>A
NR_027690.1:n.932+1G>A
NR_027690.2:n.930+1G>A
ENST00000339098.9:c.973+1G>A	ENSP00000341159.5:n.973+1G>A
ENST00000374967.6:c.831+1G>A	ENSP00000364106.2:n.831+1G>A
ENST00000374969.6:c.556+1G>A	ENSP00000364108.2:n.556+1G>A
ENST00000374970.6:c.688+1G>A	ENSP00000364109.2:n.688+1G>A
ENST00000409440.7:c.841+1G>A	ENSP00000387080.3:n.841+1G>A
ENST00000410087.7:c.895+1G>A	ENSP00000386725.3:n.895+1G>A
ENST00000421817.5:c.*177+1G>A	ENSP00000411466.1:n.*177+1G>A
ENST00000452174.5:c.699+1G>A	ENSP00000409198.1:n.699+1G>A
ENST00000479558.5:n.893+1G>A
ENST00000494398.5:n.895+1G>A
ENST00000684145.1:c.139+1G>A	ENSP00000508396.1:n.139+1G>A