Canonical Allele Identifier: CA1279906526

Gene: CKAP2L

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112756726A= , CM000664.2:g.112756726A=	GRCh38
NC_000002.11:g.113514303A= , CM000664.1:g.113514303A=	GRCh37
NC_000002.10:g.113230774A=	NCBI36
NG_041820.1:g.12952T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302450.11:c.645T= MANE Select	ENSP00000305204.6:p.Asn215=
ENST00000302450.10:c.645T=	ENSP00000305204.6:p.Asn215=
ENST00000435431.5:c.478+167T=	ENSP00000414834.1:n.478+167T=
NM_001304361.1:c.150T=	NP_001291290.1:p.Asn50=
NM_152515.4:c.645T=	NP_689728.3:p.Asn215=
NR_130712.1:n.557+167T=
XM_011510666.1:c.150T=	XP_011508968.1:p.Asn50=
XM_011510666.2:c.150T=	XP_011508968.1:p.Asn50=
NM_152515.5:c.645T= MANE Select	NP_689728.3:p.Asn215=
NM_001304361.2:c.150T=	NP_001291290.1:p.Asn50=
NR_130712.2:n.489+167T=