Canonical Allele Identifier: CA1918248402
Gene: NODAL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70432194C= , CM000672.2:g.70432194C= GRCh38
NC_000010.10:g.72191950C= , CM000672.1:g.72191950C= GRCh37
NC_000010.9:g.71861956C= NCBI36
NG_012448.1:g.14516G=
NG_012448.2:g.20755G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000287139.8:c.*742G= MANE Select ENSP00000287139.3:n.*742G=
NM_018055.4:c.*742G= NP_060525.3:n.*742G=
NM_001329906.1:c.*742G= NP_001316835.1:n.*742G=
NM_018055.5:c.*742G= MANE Select NP_060525.3:n.*742G=
NM_001329906.2:c.*742G= NP_001316835.1:n.*742G=