Canonical Allele Identifier: CA1892292455

Gene: CDNF

Genomic Alleles

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

Transcript Alleles

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