Canonical Allele Identifier: CA1279906582

Gene: CKAP2L

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112756862T= , CM000664.2:g.112756862T=	GRCh38
NC_000002.11:g.113514439T= , CM000664.1:g.113514439T=	GRCh37
NC_000002.10:g.113230910T=	NCBI36
NG_041820.1:g.12816A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302450.11:c.509A= MANE Select	ENSP00000305204.6:p.His170=
ENST00000302450.10:c.509A=	ENSP00000305204.6:p.His170=
ENST00000435431.5:c.478+31A=	ENSP00000414834.1:n.478+31A=
ENST00000481732.5:n.470A=
NM_001304361.1:c.14A=	NP_001291290.1:p.His5=
NM_152515.4:c.509A=	NP_689728.3:p.His170=
NR_130712.1:n.557+31A=
XM_011510666.1:c.14A=	XP_011508968.1:p.His5=
XM_011510666.2:c.14A=	XP_011508968.1:p.His5=
NM_152515.5:c.509A= MANE Select	NP_689728.3:p.His170=
NM_001304361.2:c.14A=	NP_001291290.1:p.His5=
NR_130712.2:n.489+31A=