Canonical Allele Identifier: CA1279906485

Gene: CKAP2L

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112756619_112756620delinsCT , CM000664.2:g.112756619_112756620delinsCT	GRCh38
NC_000002.11:g.113514196_113514197delinsCT , CM000664.1:g.113514196_113514197delinsCT	GRCh37
NC_000002.10:g.113230667_113230668delinsCT	NCBI36
NG_041820.1:g.13058_13059delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302450.11:c.751_752delinsAG MANE Select	ENSP00000305204.6:p.Ser251=
ENST00000302450.10:c.751_752delinsAG	ENSP00000305204.6:p.Ser251=
ENST00000435431.5:c.478+273_478+274delinsAG	ENSP00000414834.1:n.478+273_478+274delinsAG
NM_001304361.1:c.256_257delinsAG	NP_001291290.1:p.Ser86=
NM_152515.4:c.751_752delinsAG	NP_689728.3:p.Ser251=
NR_130712.1:n.557+273_557+274delinsAG
XM_011510666.1:c.256_257delinsAG	XP_011508968.1:p.Ser86=
XM_011510666.2:c.256_257delinsAG	XP_011508968.1:p.Ser86=
NM_152515.5:c.751_752delinsAG MANE Select	NP_689728.3:p.Ser251=
NM_001304361.2:c.256_257delinsAG	NP_001291290.1:p.Ser86=
NR_130712.2:n.489+273_489+274delinsAG