Canonical Allele Identifier: CA470279258
Gene: NODAL HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.72195195C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70435439C>T , CM000672.2:g.70435439C>T GRCh38
NC_000010.10:g.72195195C>T , CM000672.1:g.72195195C>T GRCh37
NC_000010.9:g.71865201C>T NCBI36
NG_012448.1:g.11271G>A
NG_012448.2:g.17510G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000287139.8:c.738G>A MANE Select ENSP00000287139.3:p.Leu246=
ENST00000287139.7:c.738G>A ENSP00000287139.3:p.Leu246=
ENST00000414871.1:c.573G>A ENSP00000394468.1:p.Leu191=
NM_018055.4:c.738G>A NP_060525.3:p.Leu246=
NM_001329906.1:c.339G>A NP_001316835.1:p.Leu113=
XM_024448028.1:c.339G>A XP_024303796.1:p.Leu113=
NM_018055.5:c.738G>A MANE Select NP_060525.3:p.Leu246=
NM_001329906.2:c.339G>A NP_001316835.1:p.Leu113=