Canonical Allele Identifier: CA1279906525

Gene: CKAP2L

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112756724T= , CM000664.2:g.112756724T=	GRCh38
NC_000002.11:g.113514301T= , CM000664.1:g.113514301T=	GRCh37
NC_000002.10:g.113230772T=	NCBI36
NG_041820.1:g.12954A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302450.11:c.647A= MANE Select	ENSP00000305204.6:p.Gln216=
ENST00000302450.10:c.647A=	ENSP00000305204.6:p.Gln216=
ENST00000435431.5:c.478+169A=	ENSP00000414834.1:n.478+169A=
NM_001304361.1:c.152A=	NP_001291290.1:p.Gln51=
NM_152515.4:c.647A=	NP_689728.3:p.Gln216=
NR_130712.1:n.557+169A=
XM_011510666.1:c.152A=	XP_011508968.1:p.Gln51=
XM_011510666.2:c.152A=	XP_011508968.1:p.Gln51=
NM_152515.5:c.647A= MANE Select	NP_689728.3:p.Gln216=
NM_001304361.2:c.152A=	NP_001291290.1:p.Gln51=
NR_130712.2:n.489+169A=