Canonical Allele Identifier: CA1918249723
Gene: NODAL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70435270A= , CM000672.2:g.70435270A= GRCh38
NC_000010.10:g.72195026A= , CM000672.1:g.72195026A= GRCh37
NC_000010.9:g.71865032A= NCBI36
NG_012448.1:g.11440T=
NG_012448.2:g.17679T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000287139.8:c.891+16T= MANE Select ENSP00000287139.3:n.891+16T=
ENST00000287139.7:c.891+16T= ENSP00000287139.3:n.891+16T=
ENST00000414871.1:c.726+16T= ENSP00000394468.1:n.726+16T=
NM_018055.4:c.891+16T= NP_060525.3:n.891+16T=
NM_001329906.1:c.492+16T= NP_001316835.1:n.492+16T=
XM_024448028.1:c.492+16T= XP_024303796.1:n.492+16T=
NM_018055.5:c.891+16T= MANE Select NP_060525.3:n.891+16T=
NM_001329906.2:c.492+16T= NP_001316835.1:n.492+16T=