Canonical Allele Identifier: CA1918248411
Gene: NODAL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70432212G= , CM000672.2:g.70432212G= GRCh38
NC_000010.10:g.72191968G= , CM000672.1:g.72191968G= GRCh37
NC_000010.9:g.71861974G= NCBI36
NG_012448.1:g.14498C=
NG_012448.2:g.20737C=

Transcript Alleles

HGVS Amino-acid change
ENST00000287139.8:c.*724C= MANE Select ENSP00000287139.3:n.*724C=
NM_018055.4:c.*724C= NP_060525.3:n.*724C=
NM_001329906.1:c.*724C= NP_001316835.1:n.*724C=
NM_018055.5:c.*724C= MANE Select NP_060525.3:n.*724C=
NM_001329906.2:c.*724C= NP_001316835.1:n.*724C=