Canonical Allele Identifier: CA376945698
Gene: NODAL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70435531C>G , CM000672.2:g.70435531C>G GRCh38
NC_000010.10:g.72195287C>G , CM000672.1:g.72195287C>G GRCh37
NC_000010.9:g.71865293C>G NCBI36
NG_012448.1:g.11179G>C
NG_012448.2:g.17418G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000287139.8:c.646G>C MANE Select ENSP00000287139.3:p.Ala216Pro
ENST00000287139.7:c.646G>C ENSP00000287139.3:p.Ala216Pro
ENST00000414871.1:c.481G>C ENSP00000394468.1:p.Ala161Pro
NM_018055.4:c.646G>C NP_060525.3:p.Ala216Pro
NM_001329906.1:c.247G>C NP_001316835.1:p.Ala83Pro
XM_024448028.1:c.247G>C XP_024303796.1:p.Ala83Pro
NM_018055.5:c.646G>C MANE Select NP_060525.3:p.Ala216Pro
NM_001329906.2:c.247G>C NP_001316835.1:p.Ala83Pro