Canonical Allele Identifier: CA376945730

Gene: NODAL

Linked Data

• MyVariant Identifiers: chr10:g.72195302T>A (hg19) ; chr10:g.70435546T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.70435546T>A , CM000672.2:g.70435546T>A	GRCh38
NC_000010.10:g.72195302T>A , CM000672.1:g.72195302T>A	GRCh37
NC_000010.9:g.71865308T>A	NCBI36
NG_012448.1:g.11164A>T
NG_012448.2:g.17403A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000287139.8:c.631A>T MANE Select	ENSP00000287139.3:p.Thr211Ser
ENST00000287139.7:c.631A>T	ENSP00000287139.3:p.Thr211Ser
ENST00000414871.1:c.466A>T	ENSP00000394468.1:p.Thr156Ser
NM_018055.4:c.631A>T	NP_060525.3:p.Thr211Ser
NM_001329906.1:c.232A>T	NP_001316835.1:p.Thr78Ser
XM_024448028.1:c.232A>T	XP_024303796.1:p.Thr78Ser
NM_018055.5:c.631A>T MANE Select	NP_060525.3:p.Thr211Ser
NM_001329906.2:c.232A>T	NP_001316835.1:p.Thr78Ser