Canonical Allele Identifier: CA2302981630
Gene: SMAD4 HGNC NCBI

Linked Data

dbSNP Id: rs1910190944

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.51067315_51067317dup , CM000680.2:g.51067315_51067317dup GRCh38
NC_000018.9:g.48593685_48593687dup , CM000680.1:g.48593685_48593687dup GRCh37
NC_000018.8:g.46847683_46847685dup NCBI36
NG_013013.2:g.104276_104278dup , LRG_318:g.104276_104278dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000588860.6:c.1308+128_1308+130dup ENSP00000465878.2:n.1308+128_1308+130dup
ENST00000589076.6:c.1308+128_1308+130dup ENSP00000466934.2:n.1308+128_1308+130dup
ENST00000589941.2:c.1308+128_1308+130dup ENSP00000465874.2:n.1308+128_1308+130dup
ENST00000590061.2:c.1308+128_1308+130dup ENSP00000464772.2:n.1308+128_1308+130dup
ENST00000593223.2:c.1308+128_1308+130dup ENSP00000466118.2:n.1308+128_1308+130dup
ENST00000611848.2:c.1308+128_1308+130dup ENSP00000478613.2:n.1308+128_1308+130dup
ENST00000684953.1:n.2680+128_2680+130dup
ENST00000685090.1:n.1759+128_1759+130dup
ENST00000685232.1:n.1416+128_1416+130dup
ENST00000688574.1:n.1416+128_1416+130dup
ENST00000691124.1:n.2790+128_2790+130dup
ENST00000342988.8:c.1308+128_1308+130dup MANE Select ENSP00000341551.3:n.1308+128_1308+130dup
ENST00000342988.7:c.1308+128_1308+130dup ENSP00000341551.3:n.1308+128_1308+130dup
ENST00000398417.6:c.1308+128_1308+130dup ENSP00000381452.1:n.1308+128_1308+130dup
ENST00000588745.5:c.1020+128_1020+130dup ENSP00000464901.1:n.1020+128_1020+130dup
ENST00000590499.1:n.366+128_366+130dup
ENST00000591126.5:n.3309+128_3309+130dup
ENST00000592186.5:c.955+7399_955+7401dup ENSP00000468611.1:n.955+7399_955+7401dup
ENST00000593223.1:c.75+128_75+130dup ENSP00000466118.1:n.75+128_75+130dup
ENST00000611848.1:c.508+128_508+130dup
NM_005359.5:c.1308+128_1308+130dup , LRG_318t1:c.1308+128_1308+130dup NP_005350.1:n.1308+128_1308+130dup
NM_005359.6:c.1308+128_1308+130dup MANE Select NP_005350.1:n.1308+128_1308+130dup