Canonical Allele Identifier: CA2609510493

Gene: NODAL

Linked Data

• gnomAD v4: 10-70441568-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.70441573dup , CM000672.2:g.70441573dup	GRCh38
NC_000010.10:g.72201329dup , CM000672.1:g.72201329dup	GRCh37
NC_000010.9:g.71871335dup	NCBI36
NG_012448.1:g.5141dup
NG_012448.2:g.11380dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000287139.8:c.99dup MANE Select	ENSP00000287139.3:p.Gln34AlafsTer?
ENST00000287139.7:c.99dup	ENSP00000287139.3:p.Gln34AlafsTer?
ENST00000414871.1:c.29-5586dup	ENSP00000394468.1:n.29-5586dup
NM_018055.4:c.99dup	NP_060525.3:p.Gln34AlafsTer?
NM_001329906.1:c.-206-5586dup	NP_001316835.1:n.-206-5586dup
XM_024448028.1:c.-207+462dup	XP_024303796.1:n.-207+462dup
NM_018055.5:c.99dup MANE Select	NP_060525.3:p.Gln34AlafsTer?
NM_001329906.2:c.-206-5586dup	NP_001316835.1:n.-206-5586dup