Canonical Allele Identifier: CA1892314631

Gene: CDNF

Genomic Alleles

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

Transcript Alleles

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