Canonical Allele Identifier: CA662128112

Gene: CDNF

Linked Data

• dbSNP Id: rs1311384474
• MyVariant Identifiers: chr10:g.14863805A>T (hg19) ; chr10:g.14821806A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.14821806A>T , CM000672.2:g.14821806A>T	GRCh38
NC_000010.10:g.14863805A>T , CM000672.1:g.14863805A>T	GRCh37
NC_000010.9:g.14903811A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465530.2:c.386-1648T>A MANE Select	ENSP00000419395.1:n.386-1648T>A
ENST00000378441.6:n.264-1648T>A
ENST00000378442.5:c.80-1648T>A	ENSP00000367703.1:n.80-1648T>A
ENST00000465530.1:c.386-1648T>A	ENSP00000419395.1:n.386-1648T>A
ENST00000466269.1:n.311-1648T>A
ENST00000467405.1:n.189-1648T>A
NM_001029954.2:c.386-1648T>A	NP_001025125.2:n.386-1648T>A
XM_011519488.1:c.413-1648T>A	XP_011517790.1:n.413-1648T>A
XM_011519489.1:c.371-1648T>A	XP_011517791.1:n.371-1648T>A
XM_011519488.2:c.413-1648T>A	XP_011517790.1:n.413-1648T>A
NM_001029954.3:c.386-1648T>A MANE Select	NP_001025125.2:n.386-1648T>A