Canonical Allele Identifier: CA376947060

Gene: NODAL

Linked Data

• gnomAD v4: 10-70441571-C-A
• MyVariant Identifiers: chr10:g.72201327C>A (hg19) ; chr10:g.70441571C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.70441571C>A , CM000672.2:g.70441571C>A	GRCh38
NC_000010.10:g.72201327C>A , CM000672.1:g.72201327C>A	GRCh37
NC_000010.9:g.71871333C>A	NCBI36
NG_012448.1:g.5139G>T
NG_012448.2:g.11378G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000287139.8:c.97G>T MANE Select	ENSP00000287139.3:p.Gly33Trp
ENST00000287139.7:c.97G>T	ENSP00000287139.3:p.Gly33Trp
ENST00000414871.1:c.29-5588G>T	ENSP00000394468.1:n.29-5588G>T
NM_018055.4:c.97G>T	NP_060525.3:p.Gly33Trp
NM_001329906.1:c.-206-5588G>T	NP_001316835.1:n.-206-5588G>T
XM_024448028.1:c.-207+460G>T	XP_024303796.1:n.-207+460G>T
NM_018055.5:c.97G>T MANE Select	NP_060525.3:p.Gly33Trp
NM_001329906.2:c.-206-5588G>T	NP_001316835.1:n.-206-5588G>T