Canonical Allele Identifier: CA1836810

Gene: CKAP2L

Linked Data

• dbSNP Id: rs371786477
• ExAC: 2:113514285 T / A
• gnomAD v2: 2-113514285-T-A
• gnomAD v4: 2-112756708-T-A
• MyVariant Identifiers: chr2:g.113514285T>A (hg19) ; chr2:g.112756708T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112756708T>A , CM000664.2:g.112756708T>A	GRCh38
NC_000002.11:g.113514285T>A , CM000664.1:g.113514285T>A	GRCh37
NC_000002.10:g.113230756T>A	NCBI36
NG_041820.1:g.12970A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302450.11:c.663A>T MANE Select	ENSP00000305204.6:p.Leu221Phe
ENST00000302450.10:c.663A>T	ENSP00000305204.6:p.Leu221Phe
ENST00000435431.5:c.478+185A>T	ENSP00000414834.1:n.478+185A>T
NM_001304361.1:c.168A>T	NP_001291290.1:p.Leu56Phe
NM_152515.4:c.663A>T	NP_689728.3:p.Leu221Phe
NR_130712.1:n.557+185A>T
XM_011510666.1:c.168A>T	XP_011508968.1:p.Leu56Phe
XM_011510666.2:c.168A>T	XP_011508968.1:p.Leu56Phe
NM_152515.5:c.663A>T MANE Select	NP_689728.3:p.Leu221Phe
NM_001304361.2:c.168A>T	NP_001291290.1:p.Leu56Phe
NR_130712.2:n.489+185A>T