Canonical Allele Identifier: CA1918249873
Gene: NODAL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70435642C= , CM000672.2:g.70435642C= GRCh38
NC_000010.10:g.72195398C= , CM000672.1:g.72195398C= GRCh37
NC_000010.9:g.71865404C= NCBI36
NG_012448.1:g.11068G=
NG_012448.2:g.17307G=

Transcript Alleles

HGVS Amino-acid change
ENST00000287139.8:c.535G= MANE Select ENSP00000287139.3:p.Glu179=
ENST00000287139.7:c.535G= ENSP00000287139.3:p.Glu179=
ENST00000414871.1:c.370G= ENSP00000394468.1:p.Glu124=
NM_018055.4:c.535G= NP_060525.3:p.Glu179=
NM_001329906.1:c.136G= NP_001316835.1:p.Glu46=
XM_024448028.1:c.136G= XP_024303796.1:p.Glu46=
NM_018055.5:c.535G= MANE Select NP_060525.3:p.Glu179=
NM_001329906.2:c.136G= NP_001316835.1:p.Glu46=