Canonical Allele Identifier: CA470278912

Gene: NODAL

Linked Data

• MyVariant Identifiers: chr10:g.72195411G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.70435655G>A , CM000672.2:g.70435655G>A	GRCh38
NC_000010.10:g.72195411G>A , CM000672.1:g.72195411G>A	GRCh37
NC_000010.9:g.71865417G>A	NCBI36
NG_012448.1:g.11055C>T
NG_012448.2:g.17294C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000287139.8:c.522C>T MANE Select	ENSP00000287139.3:p.Ser174=
ENST00000287139.7:c.522C>T	ENSP00000287139.3:p.Ser174=
ENST00000414871.1:c.357C>T	ENSP00000394468.1:p.Ser119=
NM_018055.4:c.522C>T	NP_060525.3:p.Ser174=
NM_001329906.1:c.123C>T	NP_001316835.1:p.Ser41=
XM_024448028.1:c.123C>T	XP_024303796.1:p.Ser41=
NM_018055.5:c.522C>T MANE Select	NP_060525.3:p.Ser174=
NM_001329906.2:c.123C>T	NP_001316835.1:p.Ser41=