Canonical Allele Identifier: CA2302971711

Gene: SMAD4

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.51046908T= , CM000680.2:g.51046908T=	GRCh38
NC_000018.9:g.48573278T= , CM000680.1:g.48573278T=	GRCh37
NC_000018.8:g.46827276T=	NCBI36
NG_013013.2:g.83869T= , LRG_318:g.83869T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588860.6:c.-127-12T=	ENSP00000465878.2:n.-127-12T=
ENST00000589076.6:c.-127-12T=	ENSP00000466934.2:n.-127-12T=
ENST00000589941.2:c.-127-12T=	ENSP00000465874.2:n.-127-12T=
ENST00000590061.2:c.-59-80T=	ENSP00000464772.2:n.-59-80T=
ENST00000593223.2:c.-127-12T=	ENSP00000466118.2:n.-127-12T=
ENST00000342988.8:c.-127-12T= MANE Select	ENSP00000341551.3:n.-127-12T=
ENST00000342988.7:c.-127-12T=	ENSP00000341551.3:n.-127-12T=
ENST00000398417.6:c.-127-12T=	ENSP00000381452.1:n.-127-12T=
ENST00000588256.1:n.335-12T=
ENST00000588860.5:c.-127-12T=	ENSP00000465878.1:n.-127-12T=
ENST00000589076.5:c.-127-12T=	ENSP00000466934.1:n.-127-12T=
ENST00000589941.1:c.-127-12T=	ENSP00000465874.1:n.-127-12T=
ENST00000590061.1:c.-59-80T=	ENSP00000464772.1:n.-59-80T=
ENST00000590722.2:c.158-12T=	ENSP00000465737.1:n.158-12T=
ENST00000591914.5:c.-127-12T=	ENSP00000466941.1:n.-127-12T=
ENST00000592911.5:n.28-1778T=
NM_005359.5:c.-127-12T= , LRG_318t1:c.-127-12T=	NP_005350.1:n.-127-12T=
NM_005359.6:c.-127-12T= MANE Select	NP_005350.1:n.-127-12T=