Canonical Allele Identifier: CA348298142

Gene: CKAP2L

Linked Data

• COSMIC: COSM714724
• MyVariant Identifiers: chr2:g.113514469C>A (hg19) ; chr2:g.112756892C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112756892C>A , CM000664.2:g.112756892C>A	GRCh38
NC_000002.11:g.113514469C>A , CM000664.1:g.113514469C>A	GRCh37
NC_000002.10:g.113230940C>A	NCBI36
NG_041820.1:g.12786G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302450.11:c.479G>T MANE Select	ENSP00000305204.6:p.Gly160Val
ENST00000302450.10:c.479G>T	ENSP00000305204.6:p.Gly160Val
ENST00000435431.5:c.478+1G>T	ENSP00000414834.1:n.478+1G>T
ENST00000481732.5:n.440G>T
NM_001304361.1:c.-17G>T	NP_001291290.1:n.-17G>T
NM_152515.4:c.479G>T	NP_689728.3:p.Gly160Val
NR_130712.1:n.557+1G>T
XM_011510666.1:c.-17G>T	XP_011508968.1:n.-17G>T
XM_011510666.2:c.-17G>T	XP_011508968.1:n.-17G>T
NM_152515.5:c.479G>T MANE Select	NP_689728.3:p.Gly160Val
NM_001304361.2:c.-17G>T	NP_001291290.1:n.-17G>T
NR_130712.2:n.489+1G>T