Canonical Allele Identifier: CA13183039

Gene: CDNF

Linked Data

• dbSNP Id: rs7900873
• gnomAD v2: 10-14863864-G-A
• gnomAD v3: 10-14821865-G-A
• gnomAD v4: 10-14821865-G-A
• MyVariant Identifiers: chr10:g.14863864G>A (hg19) ; chr10:g.14821865G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.14821865G>A , CM000672.2:g.14821865G>A	GRCh38
NC_000010.10:g.14863864G>A , CM000672.1:g.14863864G>A	GRCh37
NC_000010.9:g.14903870G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000465530.2:c.386-1707C>T MANE Select	ENSP00000419395.1:n.386-1707C>T
ENST00000378441.6:n.264-1707C>T
ENST00000378442.5:c.80-1707C>T	ENSP00000367703.1:n.80-1707C>T
ENST00000465530.1:c.386-1707C>T	ENSP00000419395.1:n.386-1707C>T
ENST00000466269.1:n.311-1707C>T
ENST00000467405.1:n.189-1707C>T
NM_001029954.2:c.386-1707C>T	NP_001025125.2:n.386-1707C>T
XM_011519488.1:c.413-1707C>T	XP_011517790.1:n.413-1707C>T
XM_011519489.1:c.371-1707C>T	XP_011517791.1:n.371-1707C>T
XM_011519488.2:c.413-1707C>T	XP_011517790.1:n.413-1707C>T
NM_001029954.3:c.386-1707C>T MANE Select	NP_001025125.2:n.386-1707C>T