Canonical Allele Identifier: CA1279906491

Gene: CKAP2L

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112756631C= , CM000664.2:g.112756631C=	GRCh38
NC_000002.11:g.113514208C= , CM000664.1:g.113514208C=	GRCh37
NC_000002.10:g.113230679C=	NCBI36
NG_041820.1:g.13047G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302450.11:c.740G= MANE Select	ENSP00000305204.6:p.Gly247=
ENST00000302450.10:c.740G=	ENSP00000305204.6:p.Gly247=
ENST00000435431.5:c.478+262G=	ENSP00000414834.1:n.478+262G=
NM_001304361.1:c.245G=	NP_001291290.1:p.Gly82=
NM_152515.4:c.740G=	NP_689728.3:p.Gly247=
NR_130712.1:n.557+262G=
XM_011510666.1:c.245G=	XP_011508968.1:p.Gly82=
XM_011510666.2:c.245G=	XP_011508968.1:p.Gly82=
NM_152515.5:c.740G= MANE Select	NP_689728.3:p.Gly247=
NM_001304361.2:c.245G=	NP_001291290.1:p.Gly82=
NR_130712.2:n.489+262G=