Canonical Allele Identifier: CA1918249869
Gene: NODAL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70435631C= , CM000672.2:g.70435631C= GRCh38
NC_000010.10:g.72195387C= , CM000672.1:g.72195387C= GRCh37
NC_000010.9:g.71865393C= NCBI36
NG_012448.1:g.11079G=
NG_012448.2:g.17318G=

Transcript Alleles

HGVS Amino-acid change
ENST00000287139.8:c.546G= MANE Select ENSP00000287139.3:p.Pro182=
ENST00000287139.7:c.546G= ENSP00000287139.3:p.Pro182=
ENST00000414871.1:c.381G= ENSP00000394468.1:p.Pro127=
NM_018055.4:c.546G= NP_060525.3:p.Pro182=
NM_001329906.1:c.147G= NP_001316835.1:p.Pro49=
XM_024448028.1:c.147G= XP_024303796.1:p.Pro49=
NM_018055.5:c.546G= MANE Select NP_060525.3:p.Pro182=
NM_001329906.2:c.147G= NP_001316835.1:p.Pro49=