Canonical Allele Identifier: CA1279906591

Gene: CKAP2L

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112756892C= , CM000664.2:g.112756892C=	GRCh38
NC_000002.11:g.113514469C= , CM000664.1:g.113514469C=	GRCh37
NC_000002.10:g.113230940C=	NCBI36
NG_041820.1:g.12786G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302450.11:c.479G= MANE Select	ENSP00000305204.6:p.Gly160=
ENST00000302450.10:c.479G=	ENSP00000305204.6:p.Gly160=
ENST00000435431.5:c.478+1G=	ENSP00000414834.1:n.478+1G=
ENST00000481732.5:n.440G=
NM_001304361.1:c.-17G=	NP_001291290.1:n.-17G=
NM_152515.4:c.479G=	NP_689728.3:p.Gly160=
NR_130712.1:n.557+1G=
XM_011510666.1:c.-17G=	XP_011508968.1:n.-17G=
XM_011510666.2:c.-17G=	XP_011508968.1:n.-17G=
NM_152515.5:c.479G= MANE Select	NP_689728.3:p.Gly160=
NM_001304361.2:c.-17G=	NP_001291290.1:n.-17G=
NR_130712.2:n.489+1G=