Canonical Allele Identifier: CA1279906584

Gene: CKAP2L

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112756869T= , CM000664.2:g.112756869T=	GRCh38
NC_000002.11:g.113514446T= , CM000664.1:g.113514446T=	GRCh37
NC_000002.10:g.113230917T=	NCBI36
NG_041820.1:g.12809A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302450.11:c.502A= MANE Select	ENSP00000305204.6:p.Asn168=
ENST00000302450.10:c.502A=	ENSP00000305204.6:p.Asn168=
ENST00000435431.5:c.478+24A=	ENSP00000414834.1:n.478+24A=
ENST00000481732.5:n.463A=
NM_001304361.1:c.7A=	NP_001291290.1:p.Asn3=
NM_152515.4:c.502A=	NP_689728.3:p.Asn168=
NR_130712.1:n.557+24A=
XM_011510666.1:c.7A=	XP_011508968.1:p.Asn3=
XM_011510666.2:c.7A=	XP_011508968.1:p.Asn3=
NM_152515.5:c.502A= MANE Select	NP_689728.3:p.Asn168=
NM_001304361.2:c.7A=	NP_001291290.1:p.Asn3=
NR_130712.2:n.489+24A=