Canonical Allele Identifier: CA1836812
Gene: CKAP2L HGNC NCBI

Linked Data

dbSNP Id: rs371752157

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112756724T>G , CM000664.2:g.112756724T>G GRCh38
NC_000002.11:g.113514301T>G , CM000664.1:g.113514301T>G GRCh37
NC_000002.10:g.113230772T>G NCBI36
NG_041820.1:g.12954A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000302450.11:c.647A>C MANE Select ENSP00000305204.6:p.Gln216Pro
ENST00000302450.10:c.647A>C ENSP00000305204.6:p.Gln216Pro
ENST00000435431.5:c.478+169A>C ENSP00000414834.1:n.478+169A>C
NM_001304361.1:c.152A>C NP_001291290.1:p.Gln51Pro
NM_152515.4:c.647A>C NP_689728.3:p.Gln216Pro
NR_130712.1:n.557+169A>C
XM_011510666.1:c.152A>C XP_011508968.1:p.Gln51Pro
XM_011510666.2:c.152A>C XP_011508968.1:p.Gln51Pro
NM_152515.5:c.647A>C MANE Select NP_689728.3:p.Gln216Pro
NM_001304361.2:c.152A>C NP_001291290.1:p.Gln51Pro
NR_130712.2:n.489+169A>C