Canonical Allele Identifier: CA1918248405
Gene: NODAL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70432199T= , CM000672.2:g.70432199T= GRCh38
NC_000010.10:g.72191955T= , CM000672.1:g.72191955T= GRCh37
NC_000010.9:g.71861961T= NCBI36
NG_012448.1:g.14511A=
NG_012448.2:g.20750A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000287139.8:c.*737A= MANE Select ENSP00000287139.3:n.*737A=
NM_018055.4:c.*737A= NP_060525.3:n.*737A=
NM_001329906.1:c.*737A= NP_001316835.1:n.*737A=
NM_018055.5:c.*737A= MANE Select NP_060525.3:n.*737A=
NM_001329906.2:c.*737A= NP_001316835.1:n.*737A=