Canonical Allele Identifier: CA1279906497

Gene: CKAP2L

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112756646T= , CM000664.2:g.112756646T=	GRCh38
NC_000002.11:g.113514223T= , CM000664.1:g.113514223T=	GRCh37
NC_000002.10:g.113230694T=	NCBI36
NG_041820.1:g.13032A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302450.11:c.725A= MANE Select	ENSP00000305204.6:p.Asn242=
ENST00000302450.10:c.725A=	ENSP00000305204.6:p.Asn242=
ENST00000435431.5:c.478+247A=	ENSP00000414834.1:n.478+247A=
NM_001304361.1:c.230A=	NP_001291290.1:p.Asn77=
NM_152515.4:c.725A=	NP_689728.3:p.Asn242=
NR_130712.1:n.557+247A=
XM_011510666.1:c.230A=	XP_011508968.1:p.Asn77=
XM_011510666.2:c.230A=	XP_011508968.1:p.Asn77=
NM_152515.5:c.725A= MANE Select	NP_689728.3:p.Asn242=
NM_001304361.2:c.230A=	NP_001291290.1:p.Asn77=
NR_130712.2:n.489+247A=