Canonical Allele Identifier: CA1892311066

Gene: CDNF

Linked Data

• dbSNP Id: rs1833740785

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.14821824T>C , CM000672.2:g.14821824T>C	GRCh38
NC_000010.10:g.14863823T>C , CM000672.1:g.14863823T>C	GRCh37
NC_000010.9:g.14903829T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465530.2:c.386-1666A>G MANE Select	ENSP00000419395.1:n.386-1666A>G
ENST00000378441.6:n.264-1666A>G
ENST00000378442.5:c.80-1666A>G	ENSP00000367703.1:n.80-1666A>G
ENST00000465530.1:c.386-1666A>G	ENSP00000419395.1:n.386-1666A>G
ENST00000466269.1:n.311-1666A>G
ENST00000467405.1:n.189-1666A>G
NM_001029954.2:c.386-1666A>G	NP_001025125.2:n.386-1666A>G
XM_011519488.1:c.413-1666A>G	XP_011517790.1:n.413-1666A>G
XM_011519489.1:c.371-1666A>G	XP_011517791.1:n.371-1666A>G
XM_011519488.2:c.413-1666A>G	XP_011517790.1:n.413-1666A>G
NM_001029954.3:c.386-1666A>G MANE Select	NP_001025125.2:n.386-1666A>G