Canonical Allele Identifier: CA2735217997
Gene: SMAD4 HGNC NCBI

Linked Data

dbSNP Id: rs2144489517

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.51083973dup , CM000680.2:g.51083973dup GRCh38
NC_000018.9:g.48610343dup , CM000680.1:g.48610343dup GRCh37
NC_000018.8:g.46864341dup NCBI36
NG_013013.2:g.120934dup , LRG_318:g.120934dup

Transcript Alleles

HGVS Amino-acid change
ENST00000588860.6:c.*5506dup ENSP00000465878.2:n.*5506dup
ENST00000589076.6:c.*5506dup ENSP00000466934.2:n.*5506dup
ENST00000589941.2:c.*5506dup ENSP00000465874.2:n.*5506dup
ENST00000590061.2:c.*5506dup ENSP00000464772.2:n.*5506dup
ENST00000688574.1:n.7273dup
ENST00000342988.8:c.*5506dup MANE Select ENSP00000341551.3:n.*5506dup
ENST00000342988.7:c.*5506dup ENSP00000341551.3:n.*5506dup
ENST00000398417.6:c.*5506dup ENSP00000381452.1:n.*5506dup
NM_005359.5:c.*5506dup , LRG_318t1:c.*5506dup NP_005350.1:n.*5506dup
NM_005359.6:c.*5506dup MANE Select NP_005350.1:n.*5506dup