Canonical Allele Identifier: CA1918249824
Gene: NODAL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70435529G= , CM000672.2:g.70435529G= GRCh38
NC_000010.10:g.72195285G= , CM000672.1:g.72195285G= GRCh37
NC_000010.9:g.71865291G= NCBI36
NG_012448.1:g.11181C=
NG_012448.2:g.17420C=

Transcript Alleles

HGVS Amino-acid change
ENST00000287139.8:c.648C= MANE Select ENSP00000287139.3:p.Ala216=
ENST00000287139.7:c.648C= ENSP00000287139.3:p.Ala216=
ENST00000414871.1:c.483C= ENSP00000394468.1:p.Ala161=
NM_018055.4:c.648C= NP_060525.3:p.Ala216=
NM_001329906.1:c.249C= NP_001316835.1:p.Ala83=
XM_024448028.1:c.249C= XP_024303796.1:p.Ala83=
NM_018055.5:c.648C= MANE Select NP_060525.3:p.Ala216=
NM_001329906.2:c.249C= NP_001316835.1:p.Ala83=