Canonical Allele Identifier: CA2574571352

Gene: NODAL

Linked Data

• gnomAD v4: 10-70435262-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.70435262T>C , CM000672.2:g.70435262T>C	GRCh38
NC_000010.10:g.72195018T>C , CM000672.1:g.72195018T>C	GRCh37
NC_000010.9:g.71865024T>C	NCBI36
NG_012448.1:g.11448A>G
NG_012448.2:g.17687A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000287139.8:c.891+24A>G MANE Select	ENSP00000287139.3:n.891+24A>G
ENST00000287139.7:c.891+24A>G	ENSP00000287139.3:n.891+24A>G
ENST00000414871.1:c.726+24A>G	ENSP00000394468.1:n.726+24A>G
NM_018055.4:c.891+24A>G	NP_060525.3:n.891+24A>G
NM_001329906.1:c.492+24A>G	NP_001316835.1:n.492+24A>G
XM_024448028.1:c.492+24A>G	XP_024303796.1:n.492+24A>G
NM_018055.5:c.891+24A>G MANE Select	NP_060525.3:n.891+24A>G
NM_001329906.2:c.492+24A>G	NP_001316835.1:n.492+24A>G