Canonical Allele Identifier: CA470279266

Gene: NODAL

Linked Data

• dbSNP Id: rs1444321917
• gnomAD v3: 10-70435442-T-C
• gnomAD v4: 10-70435442-T-C
• MyVariant Identifiers: chr10:g.72195198T>C (hg19) ; chr10:g.70435442T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.70435442T>C , CM000672.2:g.70435442T>C	GRCh38
NC_000010.10:g.72195198T>C , CM000672.1:g.72195198T>C	GRCh37
NC_000010.9:g.71865204T>C	NCBI36
NG_012448.1:g.11268A>G
NG_012448.2:g.17507A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000287139.8:c.735A>G MANE Select	ENSP00000287139.3:p.Gln245=
ENST00000287139.7:c.735A>G	ENSP00000287139.3:p.Gln245=
ENST00000414871.1:c.570A>G	ENSP00000394468.1:p.Gln190=
NM_018055.4:c.735A>G	NP_060525.3:p.Gln245=
NM_001329906.1:c.336A>G	NP_001316835.1:p.Gln112=
XM_024448028.1:c.336A>G	XP_024303796.1:p.Gln112=
NM_018055.5:c.735A>G MANE Select	NP_060525.3:p.Gln245=
NM_001329906.2:c.336A>G	NP_001316835.1:p.Gln112=