Canonical Allele Identifier: CA1279906538

Gene: CKAP2L

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112756757G= , CM000664.2:g.112756757G=	GRCh38
NC_000002.11:g.113514334G= , CM000664.1:g.113514334G=	GRCh37
NC_000002.10:g.113230805G=	NCBI36
NG_041820.1:g.12921C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302450.11:c.614C= MANE Select	ENSP00000305204.6:p.Thr205=
ENST00000302450.10:c.614C=	ENSP00000305204.6:p.Thr205=
ENST00000435431.5:c.478+136C=	ENSP00000414834.1:n.478+136C=
NM_001304361.1:c.119C=	NP_001291290.1:p.Thr40=
NM_152515.4:c.614C=	NP_689728.3:p.Thr205=
NR_130712.1:n.557+136C=
XM_011510666.1:c.119C=	XP_011508968.1:p.Thr40=
XM_011510666.2:c.119C=	XP_011508968.1:p.Thr40=
NM_152515.5:c.614C= MANE Select	NP_689728.3:p.Thr205=
NM_001304361.2:c.119C=	NP_001291290.1:p.Thr40=
NR_130712.2:n.489+136C=