Canonical Allele Identifier: CA348297619

Gene: CKAP2L

Linked Data

• COSMIC: COSM5483062
• MyVariant Identifiers: chr2:g.113514239G>C (hg19) ; chr2:g.112756662G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112756662G>C , CM000664.2:g.112756662G>C	GRCh38
NC_000002.11:g.113514239G>C , CM000664.1:g.113514239G>C	GRCh37
NC_000002.10:g.113230710G>C	NCBI36
NG_041820.1:g.13016C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302450.11:c.709C>G MANE Select	ENSP00000305204.6:p.Leu237Val
ENST00000302450.10:c.709C>G	ENSP00000305204.6:p.Leu237Val
ENST00000435431.5:c.478+231C>G	ENSP00000414834.1:n.478+231C>G
NM_001304361.1:c.214C>G	NP_001291290.1:p.Leu72Val
NM_152515.4:c.709C>G	NP_689728.3:p.Leu237Val
NR_130712.1:n.557+231C>G
XM_011510666.1:c.214C>G	XP_011508968.1:p.Leu72Val
XM_011510666.2:c.214C>G	XP_011508968.1:p.Leu72Val
NM_152515.5:c.709C>G MANE Select	NP_689728.3:p.Leu237Val
NM_001304361.2:c.214C>G	NP_001291290.1:p.Leu72Val
NR_130712.2:n.489+231C>G