Canonical Allele Identifier: CA1918249721
Gene: NODAL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70435268T= , CM000672.2:g.70435268T= GRCh38
NC_000010.10:g.72195024T= , CM000672.1:g.72195024T= GRCh37
NC_000010.9:g.71865030T= NCBI36
NG_012448.1:g.11442A=
NG_012448.2:g.17681A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000287139.8:c.891+18A= MANE Select ENSP00000287139.3:n.891+18A=
ENST00000287139.7:c.891+18A= ENSP00000287139.3:n.891+18A=
ENST00000414871.1:c.726+18A= ENSP00000394468.1:n.726+18A=
NM_018055.4:c.891+18A= NP_060525.3:n.891+18A=
NM_001329906.1:c.492+18A= NP_001316835.1:n.492+18A=
XM_024448028.1:c.492+18A= XP_024303796.1:n.492+18A=
NM_018055.5:c.891+18A= MANE Select NP_060525.3:n.891+18A=
NM_001329906.2:c.492+18A= NP_001316835.1:n.492+18A=