Canonical Allele Identifier: CA1279906581

Gene: CKAP2L

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112756860C= , CM000664.2:g.112756860C=	GRCh38
NC_000002.11:g.113514437C= , CM000664.1:g.113514437C=	GRCh37
NC_000002.10:g.113230908C=	NCBI36
NG_041820.1:g.12818G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302450.11:c.511G= MANE Select	ENSP00000305204.6:p.Val171=
ENST00000302450.10:c.511G=	ENSP00000305204.6:p.Val171=
ENST00000435431.5:c.478+33G=	ENSP00000414834.1:n.478+33G=
ENST00000481732.5:n.472G=
NM_001304361.1:c.16G=	NP_001291290.1:p.Val6=
NM_152515.4:c.511G=	NP_689728.3:p.Val171=
NR_130712.1:n.557+33G=
XM_011510666.1:c.16G=	XP_011508968.1:p.Val6=
XM_011510666.2:c.16G=	XP_011508968.1:p.Val6=
NM_152515.5:c.511G= MANE Select	NP_689728.3:p.Val171=
NM_001304361.2:c.16G=	NP_001291290.1:p.Val6=
NR_130712.2:n.489+33G=