Canonical Allele Identifier: CA2609510312
Gene: NODAL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70432193A>T , CM000672.2:g.70432193A>T GRCh38
NC_000010.10:g.72191949A>T , CM000672.1:g.72191949A>T GRCh37
NC_000010.9:g.71861955A>T NCBI36
NG_012448.1:g.14517T>A
NG_012448.2:g.20756T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000287139.8:c.*743T>A MANE Select ENSP00000287139.3:n.*743T>A
NM_018055.4:c.*743T>A NP_060525.3:n.*743T>A
NM_001329906.1:c.*743T>A NP_001316835.1:n.*743T>A
NM_018055.5:c.*743T>A MANE Select NP_060525.3:n.*743T>A
NM_001329906.2:c.*743T>A NP_001316835.1:n.*743T>A