Canonical Allele Identifier: CA2609507836
Gene: NODAL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70435452_70435455del , CM000672.2:g.70435452_70435455del GRCh38
NC_000010.10:g.72195208_72195211del , CM000672.1:g.72195208_72195211del GRCh37
NC_000010.9:g.71865214_71865217del NCBI36
NG_012448.1:g.11259_11262del
NG_012448.2:g.17498_17501del

Transcript Alleles

HGVS Amino-acid Change
ENST00000287139.8:c.726_729del MANE Select ENSP00000287139.3:p.Asp242GlufsTer16
ENST00000287139.7:c.726_729del ENSP00000287139.3:p.Asp242GlufsTer16
ENST00000414871.1:c.561_564del ENSP00000394468.1:p.Asp187GlufsTer16
NM_018055.4:c.726_729del NP_060525.3:p.Asp242GlufsTer16
NM_001329906.1:c.327_330del NP_001316835.1:p.Asp109GlufsTer16
XM_024448028.1:c.327_330del XP_024303796.1:p.Asp109GlufsTer16
NM_018055.5:c.726_729del MANE Select NP_060525.3:p.Asp242GlufsTer16
NM_001329906.2:c.327_330del NP_001316835.1:p.Asp109GlufsTer16