Canonical Allele Identifier: CA891842303

Gene: SMAD4

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.51048815_51048824del , CM000680.2:g.51048815_51048824del	GRCh38
NC_000018.9:g.48575185_48575194del , CM000680.1:g.48575185_48575194del	GRCh37
NC_000018.8:g.46829183_46829192del	NCBI36
NG_013013.2:g.85776_85785del , LRG_318:g.85776_85785del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588860.6:c.379_388del	ENSP00000465878.2:p.Cys127HisfsTer17
ENST00000589076.6:c.379_388del	ENSP00000466934.2:p.Cys127HisfsTer17
ENST00000589941.2:c.379_388del	ENSP00000465874.2:p.Cys127HisfsTer17
ENST00000590061.2:c.379_388del	ENSP00000464772.2:p.Cys127HisfsTer17
ENST00000593223.2:c.379_388del	ENSP00000466118.2:p.Cys127HisfsTer17
ENST00000611848.2:c.379_388del	ENSP00000478613.2:p.Cys127HisfsTer17
ENST00000342988.8:c.379_388del MANE Select	ENSP00000341551.3:p.Cys127HisfsTer17
ENST00000342988.7:c.379_388del	ENSP00000341551.3:p.Cys127HisfsTer17
ENST00000398417.6:c.379_388del	ENSP00000381452.1:p.Cys127HisfsTer17
ENST00000588745.5:c.379_388del	ENSP00000464901.1:p.Cys127HisfsTer17
ENST00000589706.1:n.247_256del
ENST00000590061.1:c.379_388del	ENSP00000464772.1:p.Cys127HisfsTer?
ENST00000590722.2:c.*402_*411del	ENSP00000465737.1:n.*402_*411del
ENST00000591914.5:c.379_388del	ENSP00000466941.1:p.Cys127HisfsTer17
ENST00000592186.5:c.379_388del	ENSP00000468611.1:p.Cys127HisfsTer17
ENST00000592911.5:n.157_166del
NM_005359.5:c.379_388del , LRG_318t1:c.379_388del	NP_005350.1:p.Cys127HisfsTer17
NM_005359.6:c.379_388del MANE Select	NP_005350.1:p.Cys127HisfsTer17