Canonical Allele Identifier: CA1279906578

Gene: CKAP2L

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112756852_112756853delinsGT , CM000664.2:g.112756852_112756853delinsGT	GRCh38
NC_000002.11:g.113514429_113514430delinsGT , CM000664.1:g.113514429_113514430delinsGT	GRCh37
NC_000002.10:g.113230900_113230901delinsGT	NCBI36
NG_041820.1:g.12825_12826delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302450.11:c.518_519delinsAC MANE Select	ENSP00000305204.6:p.Asn173=
ENST00000302450.10:c.518_519delinsAC	ENSP00000305204.6:p.Asn173=
ENST00000435431.5:c.478+40_478+41delinsAC	ENSP00000414834.1:n.478+40_478+41delinsAC
ENST00000481732.5:n.479_480delinsAC
NM_001304361.1:c.23_24delinsAC	NP_001291290.1:p.Asn8=
NM_152515.4:c.518_519delinsAC	NP_689728.3:p.Asn173=
NR_130712.1:n.557+40_557+41delinsAC
XM_011510666.1:c.23_24delinsAC	XP_011508968.1:p.Asn8=
XM_011510666.2:c.23_24delinsAC	XP_011508968.1:p.Asn8=
NM_152515.5:c.518_519delinsAC MANE Select	NP_689728.3:p.Asn173=
NM_001304361.2:c.23_24delinsAC	NP_001291290.1:p.Asn8=
NR_130712.2:n.489+40_489+41delinsAC