Canonical Allele Identifier: CA402466063
Gene: SMAD4 HGNC NCBI

Linked Data

dbSNP Id: rs149755320

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.51078381A>C , CM000680.2:g.51078381A>C GRCh38
NC_000018.9:g.48604751A>C , CM000680.1:g.48604751A>C GRCh37
NC_000018.8:g.46858749A>C NCBI36
NG_013013.2:g.115342A>C , LRG_318:g.115342A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000588860.6:c.1573A>C ENSP00000465878.2:p.Ile525Leu
ENST00000589076.6:c.1573A>C ENSP00000466934.2:p.Ile525Leu
ENST00000589941.2:c.1573A>C ENSP00000465874.2:p.Ile525Leu
ENST00000590061.2:c.1573A>C ENSP00000464772.2:p.Ile525Leu
ENST00000593223.2:c.*1570A>C ENSP00000466118.2:n.*1570A>C
ENST00000611848.2:c.*225A>C ENSP00000478613.2:n.*225A>C
ENST00000684953.1:n.3588A>C
ENST00000685090.1:n.3503A>C
ENST00000685232.1:n.1794A>C
ENST00000688574.1:n.1681A>C
ENST00000691124.1:n.4534A>C
ENST00000342988.8:c.1573A>C MANE Select ENSP00000341551.3:p.Ile525Leu
ENST00000342988.7:c.1573A>C ENSP00000341551.3:p.Ile525Leu
ENST00000398417.6:c.1573A>C ENSP00000381452.1:p.Ile525Leu
ENST00000586253.1:n.295A>C
ENST00000588745.5:c.1285A>C ENSP00000464901.1:p.Ile429Leu
ENST00000591126.5:n.3574A>C
ENST00000592186.5:c.1220A>C ENSP00000468611.1:n.1220A>C
ENST00000611848.1:c.886A>C
NM_005359.5:c.1573A>C , LRG_318t1:c.1573A>C NP_005350.1:p.Ile525Leu
NM_005359.6:c.1573A>C MANE Select NP_005350.1:p.Ile525Leu