Canonical Allele Identifier: CA1279906573

Gene: CKAP2L

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112756834A= , CM000664.2:g.112756834A=	GRCh38
NC_000002.11:g.113514411A= , CM000664.1:g.113514411A=	GRCh37
NC_000002.10:g.113230882A=	NCBI36
NG_041820.1:g.12844T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302450.11:c.537T= MANE Select	ENSP00000305204.6:p.Phe179=
ENST00000302450.10:c.537T=	ENSP00000305204.6:p.Phe179=
ENST00000435431.5:c.478+59T=	ENSP00000414834.1:n.478+59T=
ENST00000481732.5:n.498T=
NM_001304361.1:c.42T=	NP_001291290.1:p.Phe14=
NM_152515.4:c.537T=	NP_689728.3:p.Phe179=
NR_130712.1:n.557+59T=
XM_011510666.1:c.42T=	XP_011508968.1:p.Phe14=
XM_011510666.2:c.42T=	XP_011508968.1:p.Phe14=
NM_152515.5:c.537T= MANE Select	NP_689728.3:p.Phe179=
NM_001304361.2:c.42T=	NP_001291290.1:p.Phe14=
NR_130712.2:n.489+59T=