Canonical Allele Identifier: CA2609507980
Gene: NODAL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70435553dup , CM000672.2:g.70435553dup GRCh38
NC_000010.10:g.72195309dup , CM000672.1:g.72195309dup GRCh37
NC_000010.9:g.71865315dup NCBI36
NG_012448.1:g.11157dup
NG_012448.2:g.17396dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000287139.8:c.624dup MANE Select ENSP00000287139.3:p.Gly209TrpfsTer?
ENST00000287139.7:c.624dup ENSP00000287139.3:p.Gly209TrpfsTer?
ENST00000414871.1:c.459dup ENSP00000394468.1:p.Gly154TrpfsTer?
NM_018055.4:c.624dup NP_060525.3:p.Gly209TrpfsTer?
NM_001329906.1:c.225dup NP_001316835.1:p.Gly76TrpfsTer?
XM_024448028.1:c.225dup XP_024303796.1:p.Gly76TrpfsTer?
NM_018055.5:c.624dup MANE Select NP_060525.3:p.Gly209TrpfsTer?
NM_001329906.2:c.225dup NP_001316835.1:p.Gly76TrpfsTer?