Canonical Allele Identifier: CA402464382
Gene: SMAD4 HGNC NCBI

Linked Data

dbSNP Id: rs2144447438

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.51065551T>C , CM000680.2:g.51065551T>C GRCh38
NC_000018.9:g.48591921T>C , CM000680.1:g.48591921T>C GRCh37
NC_000018.8:g.46845919T>C NCBI36
NG_013013.2:g.102512T>C , LRG_318:g.102512T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000588860.6:c.1084T>C ENSP00000465878.2:p.Phe362Leu
ENST00000589076.6:c.1084T>C ENSP00000466934.2:p.Phe362Leu
ENST00000589941.2:c.1084T>C ENSP00000465874.2:p.Phe362Leu
ENST00000590061.2:c.1084T>C ENSP00000464772.2:p.Phe362Leu
ENST00000593223.2:c.1084T>C ENSP00000466118.2:p.Phe362Leu
ENST00000611848.2:c.1084T>C ENSP00000478613.2:p.Phe362Leu
ENST00000684953.1:n.2456T>C
ENST00000685090.1:n.1535T>C
ENST00000685232.1:n.1192T>C
ENST00000688307.1:n.335T>C
ENST00000688574.1:n.1192T>C
ENST00000688903.1:n.1298T>C
ENST00000691124.1:n.2566T>C
ENST00000342988.8:c.1084T>C MANE Select ENSP00000341551.3:p.Phe362Leu
ENST00000342988.7:c.1084T>C ENSP00000341551.3:p.Phe362Leu
ENST00000398417.6:c.1084T>C ENSP00000381452.1:p.Phe362Leu
ENST00000588745.5:c.796T>C ENSP00000464901.1:p.Phe266Leu
ENST00000591126.5:n.3085T>C
ENST00000592186.5:c.955+5635T>C ENSP00000468611.1:n.955+5635T>C
ENST00000611848.1:c.284T>C
NM_005359.5:c.1084T>C , LRG_318t1:c.1084T>C NP_005350.1:p.Phe362Leu
NM_005359.6:c.1084T>C MANE Select NP_005350.1:p.Phe362Leu