Canonical Allele Identifier: CA1918249827
Gene: NODAL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70435540G= , CM000672.2:g.70435540G= GRCh38
NC_000010.10:g.72195296G= , CM000672.1:g.72195296G= GRCh37
NC_000010.9:g.71865302G= NCBI36
NG_012448.1:g.11170C=
NG_012448.2:g.17409C=

Transcript Alleles

HGVS Amino-acid change
ENST00000287139.8:c.637C= MANE Select ENSP00000287139.3:p.Leu213=
ENST00000287139.7:c.637C= ENSP00000287139.3:p.Leu213=
ENST00000414871.1:c.472C= ENSP00000394468.1:p.Leu158=
NM_018055.4:c.637C= NP_060525.3:p.Leu213=
NM_001329906.1:c.238C= NP_001316835.1:p.Leu80=
XM_024448028.1:c.238C= XP_024303796.1:p.Leu80=
NM_018055.5:c.637C= MANE Select NP_060525.3:p.Leu213=
NM_001329906.2:c.238C= NP_001316835.1:p.Leu80=