Canonical Allele Identifier: CA1539962563
Gene: GDNF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.37815568T= , CM000667.2:g.37815568T= GRCh38
NC_000005.9:g.37815670T= , CM000667.1:g.37815670T= GRCh37
NC_000005.8:g.37851427T= NCBI36
NG_011675.2:g.29113A=

Transcript Alleles

HGVS Amino-acid change
ENST00000326524.7:c.*83A= MANE Select ENSP00000317145.2:n.*83A=
ENST00000326524.6:c.*83A= ENSP00000317145.2:n.*83A=
ENST00000344622.8:c.*83A= ENSP00000339703.4:n.*83A=
ENST00000620847.1:c.*83A= ENSP00000478722.1:n.*83A=
NM_000514.3:c.*83A= NP_000505.1:n.*83A=
NM_001190468.1:c.*83A= NP_001177397.1:n.*83A=
NM_001190469.1:c.*83A= NP_001177398.1:n.*83A=
NM_001278098.1:c.*83A= NP_001265027.1:n.*83A=
NM_199231.2:c.*83A= NP_954701.1:n.*83A=
XM_011514028.1:c.*83A= XP_011512330.1:n.*83A=
XM_011514029.1:c.*83A= XP_011512331.1:n.*83A=
XM_011514030.1:c.*83A= XP_011512332.1:n.*83A=
XM_011514030.3:c.*83A= XP_011512332.1:n.*83A=
XM_017009337.2:c.*83A= XP_016864826.1:n.*83A=
NM_000514.4:c.*83A= MANE Select NP_000505.1:n.*83A=