Canonical Allele Identifier: CA1918249878
Gene: NODAL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70435651C= , CM000672.2:g.70435651C= GRCh38
NC_000010.10:g.72195407C= , CM000672.1:g.72195407C= GRCh37
NC_000010.9:g.71865413C= NCBI36
NG_012448.1:g.11059G=
NG_012448.2:g.17298G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000287139.8:c.526G= MANE Select ENSP00000287139.3:p.Val176=
ENST00000287139.7:c.526G= ENSP00000287139.3:p.Val176=
ENST00000414871.1:c.361G= ENSP00000394468.1:p.Val121=
NM_018055.4:c.526G= NP_060525.3:p.Val176=
NM_001329906.1:c.127G= NP_001316835.1:p.Val43=
XM_024448028.1:c.127G= XP_024303796.1:p.Val43=
NM_018055.5:c.526G= MANE Select NP_060525.3:p.Val176=
NM_001329906.2:c.127G= NP_001316835.1:p.Val43=