Canonical Allele Identifier: CA1918249717

Gene: NODAL

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.70435265_70435272delinsCCCTCACG , CM000672.2:g.70435265_70435272delinsCCCTCACG	GRCh38
NC_000010.10:g.72195021_72195028delinsCCCTCACG , CM000672.1:g.72195021_72195028delinsCCCTCACG	GRCh37
NC_000010.9:g.71865027_71865034delinsCCCTCACG	NCBI36
NG_012448.1:g.11438_11445delinsCGTGAGGG
NG_012448.2:g.17677_17684delinsCGTGAGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000287139.8:c.891+14_891+21delinsCGTGAGGG MANE Select	ENSP00000287139.3:n.891+14_891+21delinsCGTGAGGG
ENST00000287139.7:c.891+14_891+21delinsCGTGAGGG	ENSP00000287139.3:n.891+14_891+21delinsCGTGAGGG
ENST00000414871.1:c.726+14_726+21delinsCGTGAGGG	ENSP00000394468.1:n.726+14_726+21delinsCGTGAGGG
NM_018055.4:c.891+14_891+21delinsCGTGAGGG	NP_060525.3:n.891+14_891+21delinsCGTGAGGG
NM_001329906.1:c.492+14_492+21delinsCGTGAGGG	NP_001316835.1:n.492+14_492+21delinsCGTGAGGG
XM_024448028.1:c.492+14_492+21delinsCGTGAGGG	XP_024303796.1:n.492+14_492+21delinsCGTGAGGG
NM_018055.5:c.891+14_891+21delinsCGTGAGGG MANE Select	NP_060525.3:n.891+14_891+21delinsCGTGAGGG
NM_001329906.2:c.492+14_492+21delinsCGTGAGGG	NP_001316835.1:n.492+14_492+21delinsCGTGAGGG