Canonical Allele Identifier: CA2609512235
Gene: NODAL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70435267dup , CM000672.2:g.70435267dup GRCh38
NC_000010.10:g.72195023dup , CM000672.1:g.72195023dup GRCh37
NC_000010.9:g.71865029dup NCBI36
NG_012448.1:g.11447dup
NG_012448.2:g.17686dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000287139.8:c.891+23dup MANE Select ENSP00000287139.3:n.891+23dup
ENST00000287139.7:c.891+23dup ENSP00000287139.3:n.891+23dup
ENST00000414871.1:c.726+23dup ENSP00000394468.1:n.726+23dup
NM_018055.4:c.891+23dup NP_060525.3:n.891+23dup
NM_001329906.1:c.492+23dup NP_001316835.1:n.492+23dup
XM_024448028.1:c.492+23dup XP_024303796.1:n.492+23dup
NM_018055.5:c.891+23dup MANE Select NP_060525.3:n.891+23dup
NM_001329906.2:c.492+23dup NP_001316835.1:n.492+23dup