Canonical Allele Identifier: CA348297711

Gene: CKAP2L

Linked Data

• gnomAD v4: 2-112756704-G-T
• COSMIC: COSM6217966
• MyVariant Identifiers: chr2:g.113514281G>T (hg19) ; chr2:g.112756704G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112756704G>T , CM000664.2:g.112756704G>T	GRCh38
NC_000002.11:g.113514281G>T , CM000664.1:g.113514281G>T	GRCh37
NC_000002.10:g.113230752G>T	NCBI36
NG_041820.1:g.12974C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302450.11:c.667C>A MANE Select	ENSP00000305204.6:p.Pro223Thr
ENST00000302450.10:c.667C>A	ENSP00000305204.6:p.Pro223Thr
ENST00000435431.5:c.478+189C>A	ENSP00000414834.1:n.478+189C>A
NM_001304361.1:c.172C>A	NP_001291290.1:p.Pro58Thr
NM_152515.4:c.667C>A	NP_689728.3:p.Pro223Thr
NR_130712.1:n.557+189C>A
XM_011510666.1:c.172C>A	XP_011508968.1:p.Pro58Thr
XM_011510666.2:c.172C>A	XP_011508968.1:p.Pro58Thr
NM_152515.5:c.667C>A MANE Select	NP_689728.3:p.Pro223Thr
NM_001304361.2:c.172C>A	NP_001291290.1:p.Pro58Thr
NR_130712.2:n.489+189C>A