Canonical Allele Identifier: CA2609512234
Gene: NODAL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70435262del , CM000672.2:g.70435262del GRCh38
NC_000010.10:g.72195018del , CM000672.1:g.72195018del GRCh37
NC_000010.9:g.71865024del NCBI36
NG_012448.1:g.11448del
NG_012448.2:g.17687del

Transcript Alleles

HGVS Amino-acid Change
ENST00000287139.8:c.891+24del MANE Select ENSP00000287139.3:n.891+24del
ENST00000287139.7:c.891+24del ENSP00000287139.3:n.891+24del
ENST00000414871.1:c.726+24del ENSP00000394468.1:n.726+24del
NM_018055.4:c.891+24del NP_060525.3:n.891+24del
NM_001329906.1:c.492+24del NP_001316835.1:n.492+24del
XM_024448028.1:c.492+24del XP_024303796.1:n.492+24del
NM_018055.5:c.891+24del MANE Select NP_060525.3:n.891+24del
NM_001329906.2:c.492+24del NP_001316835.1:n.492+24del