Canonical Allele Identifier: CA2302986756
Gene: SMAD4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.51078020A= , CM000680.2:g.51078020A= GRCh38
NC_000018.9:g.48604390A= , CM000680.1:g.48604390A= GRCh37
NC_000018.8:g.46858388A= NCBI36
NG_013013.2:g.114981A= , LRG_318:g.114981A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000588860.6:c.1448-236A= ENSP00000465878.2:n.1448-236A=
ENST00000589076.6:c.1448-236A= ENSP00000466934.2:n.1448-236A=
ENST00000589941.2:c.1448-236A= ENSP00000465874.2:n.1448-236A=
ENST00000590061.2:c.1448-236A= ENSP00000464772.2:n.1448-236A=
ENST00000593223.2:c.*1209A= ENSP00000466118.2:n.*1209A=
ENST00000611848.2:c.*100-236A= ENSP00000478613.2:n.*100-236A=
ENST00000684953.1:n.3463-236A=
ENST00000685090.1:n.3142A=
ENST00000685232.1:n.1669-236A=
ENST00000688574.1:n.1556-236A=
ENST00000691124.1:n.4173A=
ENST00000342988.8:c.1448-236A= MANE Select ENSP00000341551.3:n.1448-236A=
ENST00000342988.7:c.1448-236A= ENSP00000341551.3:n.1448-236A=
ENST00000398417.6:c.1448-236A= ENSP00000381452.1:n.1448-236A=
ENST00000586253.1:n.170-236A=
ENST00000588745.5:c.1160-236A= ENSP00000464901.1:n.1160-236A=
ENST00000591126.5:n.3449-236A=
ENST00000592186.5:c.1095-236A= ENSP00000468611.1:n.1095-236A=
ENST00000611848.1:c.761-236A=
NM_005359.5:c.1448-236A= , LRG_318t1:c.1448-236A= NP_005350.1:n.1448-236A=
NM_005359.6:c.1448-236A= MANE Select NP_005350.1:n.1448-236A=