Canonical Allele Identifier: CA1279906589

Gene: CKAP2L

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112756886C= , CM000664.2:g.112756886C=	GRCh38
NC_000002.11:g.113514463C= , CM000664.1:g.113514463C=	GRCh37
NC_000002.10:g.113230934C=	NCBI36
NG_041820.1:g.12792G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302450.11:c.485G= MANE Select	ENSP00000305204.6:p.Cys162=
ENST00000302450.10:c.485G=	ENSP00000305204.6:p.Cys162=
ENST00000435431.5:c.478+7G=	ENSP00000414834.1:n.478+7G=
ENST00000481732.5:n.446G=
NM_001304361.1:c.-11G=	NP_001291290.1:n.-11G=
NM_152515.4:c.485G=	NP_689728.3:p.Cys162=
NR_130712.1:n.557+7G=
XM_011510666.1:c.-11G=	XP_011508968.1:n.-11G=
XM_011510666.2:c.-11G=	XP_011508968.1:n.-11G=
NM_152515.5:c.485G= MANE Select	NP_689728.3:p.Cys162=
NM_001304361.2:c.-11G=	NP_001291290.1:n.-11G=
NR_130712.2:n.489+7G=