Canonical Allele Identifier: CA1918252762
Gene: NODAL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70441612G= , CM000672.2:g.70441612G= GRCh38
NC_000010.10:g.72201368G= , CM000672.1:g.72201368G= GRCh37
NC_000010.9:g.71871374G= NCBI36
NG_012448.1:g.5098C=
NG_012448.2:g.11337C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000287139.8:c.56C= MANE Select ENSP00000287139.3:p.Ala19=
ENST00000287139.7:c.56C= ENSP00000287139.3:p.Ala19=
ENST00000414871.1:c.29-5629C= ENSP00000394468.1:n.29-5629C=
NM_018055.4:c.56C= NP_060525.3:p.Ala19=
NM_001329906.1:c.-206-5629C= NP_001316835.1:n.-206-5629C=
XM_024448028.1:c.-207+419C= XP_024303796.1:n.-207+419C=
NM_018055.5:c.56C= MANE Select NP_060525.3:p.Ala19=
NM_001329906.2:c.-206-5629C= NP_001316835.1:n.-206-5629C=
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