Canonical Allele Identifier: CA1279906571

Gene: CKAP2L

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112756828T= , CM000664.2:g.112756828T=	GRCh38
NC_000002.11:g.113514405T= , CM000664.1:g.113514405T=	GRCh37
NC_000002.10:g.113230876T=	NCBI36
NG_041820.1:g.12850A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302450.11:c.543A= MANE Select	ENSP00000305204.6:p.Lys181=
ENST00000302450.10:c.543A=	ENSP00000305204.6:p.Lys181=
ENST00000435431.5:c.478+65A=	ENSP00000414834.1:n.478+65A=
ENST00000481732.5:n.504A=
NM_001304361.1:c.48A=	NP_001291290.1:p.Lys16=
NM_152515.4:c.543A=	NP_689728.3:p.Lys181=
NR_130712.1:n.557+65A=
XM_011510666.1:c.48A=	XP_011508968.1:p.Lys16=
XM_011510666.2:c.48A=	XP_011508968.1:p.Lys16=
NM_152515.5:c.543A= MANE Select	NP_689728.3:p.Lys181=
NM_001304361.2:c.48A=	NP_001291290.1:p.Lys16=
NR_130712.2:n.489+65A=