Canonical Allele Identifier: CA376945988
Gene: NODAL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70435632G>C , CM000672.2:g.70435632G>C GRCh38
NC_000010.10:g.72195388G>C , CM000672.1:g.72195388G>C GRCh37
NC_000010.9:g.71865394G>C NCBI36
NG_012448.1:g.11078C>G
NG_012448.2:g.17317C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000287139.8:c.545C>G MANE Select ENSP00000287139.3:p.Pro182Arg
ENST00000287139.7:c.545C>G ENSP00000287139.3:p.Pro182Arg
ENST00000414871.1:c.380C>G ENSP00000394468.1:p.Pro127Arg
NM_018055.4:c.545C>G NP_060525.3:p.Pro182Arg
NM_001329906.1:c.146C>G NP_001316835.1:p.Pro49Arg
XM_024448028.1:c.146C>G XP_024303796.1:p.Pro49Arg
NM_018055.5:c.545C>G MANE Select NP_060525.3:p.Pro182Arg
NM_001329906.2:c.146C>G NP_001316835.1:p.Pro49Arg