Canonical Allele Identifier: CA1279906498

Gene: CKAP2L

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112756649A= , CM000664.2:g.112756649A=	GRCh38
NC_000002.11:g.113514226A= , CM000664.1:g.113514226A=	GRCh37
NC_000002.10:g.113230697A=	NCBI36
NG_041820.1:g.13029T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302450.11:c.722T= MANE Select	ENSP00000305204.6:p.Val241=
ENST00000302450.10:c.722T=	ENSP00000305204.6:p.Val241=
ENST00000435431.5:c.478+244T=	ENSP00000414834.1:n.478+244T=
NM_001304361.1:c.227T=	NP_001291290.1:p.Val76=
NM_152515.4:c.722T=	NP_689728.3:p.Val241=
NR_130712.1:n.557+244T=
XM_011510666.1:c.227T=	XP_011508968.1:p.Val76=
XM_011510666.2:c.227T=	XP_011508968.1:p.Val76=
NM_152515.5:c.722T= MANE Select	NP_689728.3:p.Val241=
NM_001304361.2:c.227T=	NP_001291290.1:p.Val76=
NR_130712.2:n.489+244T=