Canonical Allele Identifier: CA2302971818

Gene: SMAD4

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.51047160_51047161delinsAG , CM000680.2:g.51047160_51047161delinsAG	GRCh38
NC_000018.9:g.48573530_48573531delinsAG , CM000680.1:g.48573530_48573531delinsAG	GRCh37
NC_000018.8:g.46827528_46827529delinsAG	NCBI36
NG_013013.2:g.84121_84122delinsAG , LRG_318:g.84121_84122delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588860.6:c.114_115delinsAG	ENSP00000465878.2:p.Arg38=
ENST00000589076.6:c.114_115delinsAG	ENSP00000466934.2:p.Arg38=
ENST00000589941.2:c.114_115delinsAG	ENSP00000465874.2:p.Arg38=
ENST00000590061.2:c.114_115delinsAG	ENSP00000464772.2:p.Arg38=
ENST00000593223.2:c.114_115delinsAG	ENSP00000466118.2:p.Arg38=
ENST00000611848.2:c.114_115delinsAG	ENSP00000478613.2:p.Arg38=
ENST00000342988.8:c.114_115delinsAG MANE Select	ENSP00000341551.3:p.Arg38=
ENST00000342988.7:c.114_115delinsAG	ENSP00000341551.3:p.Arg38=
ENST00000398417.6:c.114_115delinsAG	ENSP00000381452.1:p.Arg38=
ENST00000588745.5:c.114_115delinsAG	ENSP00000464901.1:p.Arg38=
ENST00000588860.5:c.114_115delinsAG	ENSP00000465878.1:p.Arg38=
ENST00000589076.5:c.114_115delinsAG	ENSP00000466934.1:p.Arg38=
ENST00000589941.1:c.114_115delinsAG	ENSP00000465874.1:p.Arg38=
ENST00000590061.1:c.114_115delinsAG	ENSP00000464772.1:p.Arg38=
ENST00000590722.2:c.*137_*138delinsAG	ENSP00000465737.1:n.*137_*138delinsAG
ENST00000591914.5:c.114_115delinsAG	ENSP00000466941.1:p.Arg38=
ENST00000592186.5:c.114_115delinsAG	ENSP00000468611.1:p.Arg38=
ENST00000592911.5:n.28-1526_28-1525delinsAG
NM_005359.5:c.114_115delinsAG , LRG_318t1:c.114_115delinsAG	NP_005350.1:p.Arg38=
NM_005359.6:c.114_115delinsAG MANE Select	NP_005350.1:p.Arg38=