Canonical Allele Identifier: CA2010632

Gene: CERKL

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.181549621G>A , CM000664.2:g.181549621G>A	GRCh38
NC_000002.11:g.182414348G>A , CM000664.1:g.182414348G>A	GRCh37
NC_000002.10:g.182122593G>A	NCBI36
NG_021178.1:g.112487C>T
NG_021178.2:g.112487C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_201548.5:c.895+13C>T MANE Select	NP_963842.1:n.895+13C>T
ENST00000410087.8:c.895+13C>T MANE Select	ENSP00000386725.3:n.895+13C>T
NM_001030311.2:c.973+13C>T	NP_001025482.1:n.973+13C>T
NM_001030311.3:c.973+13C>T	NP_001025482.1:n.973+13C>T
NM_001030312.2:c.556+13C>T	NP_001025483.1:n.556+13C>T
NM_001030312.3:c.556+13C>T	NP_001025483.1:n.556+13C>T
NM_001030313.2:c.688+13C>T	NP_001025484.1:n.688+13C>T
NM_001030313.3:c.688+13C>T	NP_001025484.1:n.688+13C>T
NM_001160277.1:c.841+13C>T	NP_001153749.1:n.841+13C>T
NM_001160277.2:c.841+13C>T	NP_001153749.1:n.841+13C>T
NM_201548.4:c.895+13C>T	NP_963842.1:n.895+13C>T
NR_027689.1:n.800+13C>T
NR_027689.2:n.798+13C>T
NR_027690.1:n.932+13C>T
NR_027690.2:n.930+13C>T
ENST00000339098.9:c.973+13C>T	ENSP00000341159.5:n.973+13C>T
ENST00000374967.6:c.831+13C>T	ENSP00000364106.2:n.831+13C>T
ENST00000374969.6:c.556+13C>T	ENSP00000364108.2:n.556+13C>T
ENST00000374970.6:c.688+13C>T	ENSP00000364109.2:n.688+13C>T
ENST00000409440.7:c.841+13C>T	ENSP00000387080.3:n.841+13C>T
ENST00000410087.7:c.895+13C>T	ENSP00000386725.3:n.895+13C>T
ENST00000421817.5:c.*177+13C>T	ENSP00000411466.1:n.*177+13C>T
ENST00000452174.5:c.699+13C>T	ENSP00000409198.1:n.699+13C>T
ENST00000479558.5:n.893+13C>T
ENST00000494398.5:n.895+13C>T
ENST00000684145.1:c.139+13C>T	ENSP00000508396.1:n.139+13C>T