Canonical Allele Identifier: CA11926737

Gene: GDNF

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37821119C>A , CM000667.2:g.37821119C>A	GRCh38
NC_000005.9:g.37821221C>A , CM000667.1:g.37821221C>A	GRCh37
NC_000005.8:g.37856978C>A	NCBI36
NG_011675.2:g.23562G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000514.4:c.152-4984G>T MANE Select	NP_000505.1:n.152-4984G>T
ENST00000326524.7:c.152-4984G>T MANE Select	ENSP00000317145.2:n.152-4984G>T
NM_000514.3:c.152-4984G>T	NP_000505.1:n.152-4984G>T
NM_001190468.1:c.203-4984G>T	NP_001177397.1:n.203-4984G>T
NM_001190469.1:c.125-4984G>T	NP_001177398.1:n.125-4984G>T
NM_001278098.1:c.-6+2891G>T	NP_001265027.1:n.-6+2891G>T
NM_199231.2:c.74-4984G>T	NP_954701.1:n.74-4984G>T
ENST00000326524.6:c.152-4984G>T	ENSP00000317145.2:n.152-4984G>T
ENST00000344622.8:c.74-4984G>T	ENSP00000339703.4:n.74-4984G>T
ENST00000381826.8:c.125-4984G>T	ENSP00000371248.4:n.125-4984G>T
ENST00000427982.5:c.203-4984G>T	ENSP00000409007.1:n.203-4984G>T
ENST00000502572.1:c.74-4984G>T	ENSP00000423557.1:n.74-4984G>T
ENST00000510177.5:c.74-4984G>T	ENSP00000424592.1:n.74-4984G>T
ENST00000515058.5:c.74-4984G>T	ENSP00000425928.1:n.74-4984G>T
ENST00000620847.1:c.-6+2891G>T	ENSP00000478722.1:n.-6+2891G>T
XM_011514028.1:c.152-4984G>T	XP_011512330.1:n.152-4984G>T
XM_011514029.1:c.152-4984G>T	XP_011512331.1:n.152-4984G>T
XM_011514030.1:c.-5-4984G>T	XP_011512332.1:n.-5-4984G>T
XM_011514030.3:c.-5-4984G>T	XP_011512332.1:n.-5-4984G>T
XM_017009337.2:c.74-4984G>T	XP_016864826.1:n.74-4984G>T