Canonical Allele Identifier: CA203382269
Gene: CDNF HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.14830428C>A , CM000672.2:g.14830428C>A GRCh38
NC_000010.10:g.14872427C>A , CM000672.1:g.14872427C>A GRCh37
NC_000010.9:g.14912433C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000465530.2:c.116-2156G>T MANE Select ENSP00000419395.1:n.116-2156G>T
ENST00000378441.6:n.136-2156G>T
ENST00000378442.5:c.-191-2156G>T ENSP00000367703.1:n.-191-2156G>T
ENST00000465530.1:c.116-2156G>T ENSP00000419395.1:n.116-2156G>T
ENST00000466269.1:n.41-2156G>T
NM_001029954.2:c.116-2156G>T NP_001025125.2:n.116-2156G>T
XM_011519488.1:c.116-2156G>T XP_011517790.1:n.116-2156G>T
XM_011519489.1:c.116-2156G>T XP_011517791.1:n.116-2156G>T
XM_011519488.2:c.116-2156G>T XP_011517790.1:n.116-2156G>T
NM_001029954.3:c.116-2156G>T MANE Select NP_001025125.2:n.116-2156G>T
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