Canonical Allele Identifier: CA470279538
Gene: NODAL HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.72195294C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70435538C>A , CM000672.2:g.70435538C>A GRCh38
NC_000010.10:g.72195294C>A , CM000672.1:g.72195294C>A GRCh37
NC_000010.9:g.71865300C>A NCBI36
NG_012448.1:g.11172G>T
NG_012448.2:g.17411G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000287139.8:c.639G>T MANE Select ENSP00000287139.3:p.Leu213=
ENST00000287139.7:c.639G>T ENSP00000287139.3:p.Leu213=
ENST00000414871.1:c.474G>T ENSP00000394468.1:p.Leu158=
NM_018055.4:c.639G>T NP_060525.3:p.Leu213=
NM_001329906.1:c.240G>T NP_001316835.1:p.Leu80=
XM_024448028.1:c.240G>T XP_024303796.1:p.Leu80=
NM_018055.5:c.639G>T MANE Select NP_060525.3:p.Leu213=
NM_001329906.2:c.240G>T NP_001316835.1:p.Leu80=