Canonical Allele Identifier: CA1279906512

Gene: CKAP2L

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112756678_112756679delinsTG , CM000664.2:g.112756678_112756679delinsTG	GRCh38
NC_000002.11:g.113514255_113514256delinsTG , CM000664.1:g.113514255_113514256delinsTG	GRCh37
NC_000002.10:g.113230726_113230727delinsTG	NCBI36
NG_041820.1:g.12999_13000delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302450.11:c.692_693delinsCA MANE Select	ENSP00000305204.6:p.Ser231=
ENST00000302450.10:c.692_693delinsCA	ENSP00000305204.6:p.Ser231=
ENST00000435431.5:c.478+214_478+215delinsCA	ENSP00000414834.1:n.478+214_478+215delinsCA
NM_001304361.1:c.197_198delinsCA	NP_001291290.1:p.Ser66=
NM_152515.4:c.692_693delinsCA	NP_689728.3:p.Ser231=
NR_130712.1:n.557+214_557+215delinsCA
XM_011510666.1:c.197_198delinsCA	XP_011508968.1:p.Ser66=
XM_011510666.2:c.197_198delinsCA	XP_011508968.1:p.Ser66=
NM_152515.5:c.692_693delinsCA MANE Select	NP_689728.3:p.Ser231=
NM_001304361.2:c.197_198delinsCA	NP_001291290.1:p.Ser66=
NR_130712.2:n.489+214_489+215delinsCA