Canonical Allele Identifier: CA376946032
Gene: NODAL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70435640C>G , CM000672.2:g.70435640C>G GRCh38
NC_000010.10:g.72195396C>G , CM000672.1:g.72195396C>G GRCh37
NC_000010.9:g.71865402C>G NCBI36
NG_012448.1:g.11070G>C
NG_012448.2:g.17309G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000287139.8:c.537G>C MANE Select ENSP00000287139.3:p.Glu179Asp
ENST00000287139.7:c.537G>C ENSP00000287139.3:p.Glu179Asp
ENST00000414871.1:c.372G>C ENSP00000394468.1:p.Glu124Asp
NM_018055.4:c.537G>C NP_060525.3:p.Glu179Asp
NM_001329906.1:c.138G>C NP_001316835.1:p.Glu46Asp
XM_024448028.1:c.138G>C XP_024303796.1:p.Glu46Asp
NM_018055.5:c.537G>C MANE Select NP_060525.3:p.Glu179Asp
NM_001329906.2:c.138G>C NP_001316835.1:p.Glu46Asp