Canonical Allele Identifier: CA53691657
Gene: CKAP2L HGNC NCBI

Linked Data

dbSNP Id: rs1028655870

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112756818T>C , CM000664.2:g.112756818T>C GRCh38
NC_000002.11:g.113514395T>C , CM000664.1:g.113514395T>C GRCh37
NC_000002.10:g.113230866T>C NCBI36
NG_041820.1:g.12860A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000302450.11:c.553A>G MANE Select ENSP00000305204.6:p.Lys185Glu
ENST00000302450.10:c.553A>G ENSP00000305204.6:p.Lys185Glu
ENST00000435431.5:c.478+75A>G ENSP00000414834.1:n.478+75A>G
ENST00000481732.5:n.514A>G
NM_001304361.1:c.58A>G NP_001291290.1:p.Lys20Glu
NM_152515.4:c.553A>G NP_689728.3:p.Lys185Glu
NR_130712.1:n.557+75A>G
XM_011510666.1:c.58A>G XP_011508968.1:p.Lys20Glu
XM_011510666.2:c.58A>G XP_011508968.1:p.Lys20Glu
NM_152515.5:c.553A>G MANE Select NP_689728.3:p.Lys185Glu
NM_001304361.2:c.58A>G NP_001291290.1:p.Lys20Glu
NR_130712.2:n.489+75A>G