Canonical Allele Identifier: CA2302977083
Gene: SMAD4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.51058134C= , CM000680.2:g.51058134C= GRCh38
NC_000018.9:g.48584504C= , CM000680.1:g.48584504C= GRCh37
NC_000018.8:g.46838502C= NCBI36
NG_013013.2:g.95095C= , LRG_318:g.95095C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000588860.6:c.677C= ENSP00000465878.2:p.Ala226=
ENST00000589076.6:c.677C= ENSP00000466934.2:p.Ala226=
ENST00000589941.2:c.677C= ENSP00000465874.2:p.Ala226=
ENST00000590061.2:c.677C= ENSP00000464772.2:p.Ala226=
ENST00000593223.2:c.677C= ENSP00000466118.2:p.Ala226=
ENST00000611848.2:c.677C= ENSP00000478613.2:p.Ala226=
ENST00000684953.1:n.2049C=
ENST00000685232.1:n.785C=
ENST00000688307.1:n.156-1732C=
ENST00000688574.1:n.785C=
ENST00000688903.1:n.891C=
ENST00000690892.1:n.785C=
ENST00000342988.8:c.677C= MANE Select ENSP00000341551.3:p.Ala226=
ENST00000342988.7:c.677C= ENSP00000341551.3:p.Ala226=
ENST00000398417.6:c.677C= ENSP00000381452.1:p.Ala226=
ENST00000588745.5:c.667+3141C= ENSP00000464901.1:n.667+3141C=
ENST00000590722.2:c.*853C= ENSP00000465737.1:n.*853C=
ENST00000591126.5:n.2678C=
ENST00000592186.5:c.677C= ENSP00000468611.1:p.Ala226=
ENST00000592911.5:n.455C=
NM_005359.5:c.677C= , LRG_318t1:c.677C= NP_005350.1:p.Ala226=
NM_005359.6:c.677C= MANE Select NP_005350.1:p.Ala226=