Canonical Allele Identifier: CA376945695
Gene: NODAL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70435530G>T , CM000672.2:g.70435530G>T GRCh38
NC_000010.10:g.72195286G>T , CM000672.1:g.72195286G>T GRCh37
NC_000010.9:g.71865292G>T NCBI36
NG_012448.1:g.11180C>A
NG_012448.2:g.17419C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000287139.8:c.647C>A MANE Select ENSP00000287139.3:p.Ala216Asp
ENST00000287139.7:c.647C>A ENSP00000287139.3:p.Ala216Asp
ENST00000414871.1:c.482C>A ENSP00000394468.1:p.Ala161Asp
NM_018055.4:c.647C>A NP_060525.3:p.Ala216Asp
NM_001329906.1:c.248C>A NP_001316835.1:p.Ala83Asp
XM_024448028.1:c.248C>A XP_024303796.1:p.Ala83Asp
NM_018055.5:c.647C>A MANE Select NP_060525.3:p.Ala216Asp
NM_001329906.2:c.248C>A NP_001316835.1:p.Ala83Asp