Canonical Allele Identifier: CA203383990
Gene: CDNF HGNC NCBI

Linked Data

dbSNP Id: rs11259365

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.14834528G>C , CM000672.2:g.14834528G>C GRCh38
NC_000010.10:g.14876527G>C , CM000672.1:g.14876527G>C GRCh37
NC_000010.9:g.14916533G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000465530.2:c.115+3304C>G MANE Select ENSP00000419395.1:n.115+3304C>G
ENST00000378441.6:n.135+1723C>G
ENST00000378442.5:c.-308-195C>G ENSP00000367703.1:n.-308-195C>G
ENST00000465530.1:c.115+3304C>G ENSP00000419395.1:n.115+3304C>G
ENST00000466269.1:n.40+1723C>G
NM_001029954.2:c.115+3304C>G NP_001025125.2:n.115+3304C>G
XM_011519488.1:c.115+3304C>G XP_011517790.1:n.115+3304C>G
XM_011519489.1:c.115+3304C>G XP_011517791.1:n.115+3304C>G
XM_011519488.2:c.115+3304C>G XP_011517790.1:n.115+3304C>G
NM_001029954.3:c.115+3304C>G MANE Select NP_001025125.2:n.115+3304C>G