Canonical Allele Identifier: CA1836786

Gene: CKAP2L

Linked Data

• dbSNP Id: rs775471274
• ExAC: 2:113514120 C / T
• gnomAD v2: 2-113514120-C-T
• gnomAD v4: 2-112756543-C-T
• MyVariant Identifiers: chr2:g.113514120C>T (hg19) ; chr2:g.112756543C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112756543C>T , CM000664.2:g.112756543C>T	GRCh38
NC_000002.11:g.113514120C>T , CM000664.1:g.113514120C>T	GRCh37
NC_000002.10:g.113230591C>T	NCBI36
NG_041820.1:g.13135G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302450.11:c.828G>A MANE Select	ENSP00000305204.6:p.Arg276=
ENST00000302450.10:c.828G>A	ENSP00000305204.6:p.Arg276=
ENST00000435431.5:c.478+350G>A	ENSP00000414834.1:n.478+350G>A
NM_001304361.1:c.333G>A	NP_001291290.1:p.Arg111=
NM_152515.4:c.828G>A	NP_689728.3:p.Arg276=
NR_130712.1:n.557+350G>A
XM_011510666.1:c.333G>A	XP_011508968.1:p.Arg111=
XM_011510666.2:c.333G>A	XP_011508968.1:p.Arg111=
NM_152515.5:c.828G>A MANE Select	NP_689728.3:p.Arg276=
NM_001304361.2:c.333G>A	NP_001291290.1:p.Arg111=
NR_130712.2:n.489+350G>A