Canonical Allele Identifier: CA990249314
Gene: SMAD4 HGNC NCBI

Linked Data

dbSNP Id: rs1910693659
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.51084253T>A , CM000680.2:g.51084253T>A GRCh38
NC_000018.9:g.48610623T>A , CM000680.1:g.48610623T>A GRCh37
NC_000018.8:g.46864621T>A NCBI36
NG_013013.2:g.121214T>A , LRG_318:g.121214T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000588860.6:c.*5786T>A ENSP00000465878.2:n.*5786T>A
ENST00000589076.6:c.*5786T>A ENSP00000466934.2:n.*5786T>A
ENST00000589941.2:c.*5786T>A ENSP00000465874.2:n.*5786T>A
ENST00000590061.2:c.*5786T>A ENSP00000464772.2:n.*5786T>A
ENST00000688574.1:n.7553T>A
ENST00000342988.8:c.*5786T>A MANE Select ENSP00000341551.3:n.*5786T>A
ENST00000342988.7:c.*5786T>A ENSP00000341551.3:n.*5786T>A
ENST00000398417.6:c.*5786T>A ENSP00000381452.1:n.*5786T>A
NM_005359.5:c.*5786T>A , LRG_318t1:c.*5786T>A NP_005350.1:n.*5786T>A
NM_005359.6:c.*5786T>A MANE Select NP_005350.1:n.*5786T>A
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