Canonical Allele Identifier: CA1279906565

Gene: CKAP2L

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112756815_112756819delinsCTTTG , CM000664.2:g.112756815_112756819delinsCTTTG	GRCh38
NC_000002.11:g.113514392_113514396delinsCTTTG , CM000664.1:g.113514392_113514396delinsCTTTG	GRCh37
NC_000002.10:g.113230863_113230867delinsCTTTG	NCBI36
NG_041820.1:g.12859_12863delinsCAAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302450.11:c.552_556delinsCAAAG MANE Select	ENSP00000305204.6:p.Asn184=
ENST00000302450.10:c.552_556delinsCAAAG	ENSP00000305204.6:p.Asn184=
ENST00000435431.5:c.478+74_478+78delinsCAAAG	ENSP00000414834.1:n.478+74_478+78delinsCAAAG
ENST00000481732.5:n.513_517delinsCAAAG
NM_001304361.1:c.57_61delinsCAAAG	NP_001291290.1:p.Asn19=
NM_152515.4:c.552_556delinsCAAAG	NP_689728.3:p.Asn184=
NR_130712.1:n.557+74_557+78delinsCAAAG
XM_011510666.1:c.57_61delinsCAAAG	XP_011508968.1:p.Asn19=
XM_011510666.2:c.57_61delinsCAAAG	XP_011508968.1:p.Asn19=
NM_152515.5:c.552_556delinsCAAAG MANE Select	NP_689728.3:p.Asn184=
NM_001304361.2:c.57_61delinsCAAAG	NP_001291290.1:p.Asn19=
NR_130712.2:n.489+74_489+78delinsCAAAG