Canonical Allele Identifier: CA780229663

Gene: SMAD4

Linked Data

• dbSNP Id: rs1166378903
• gnomAD v3: 18-51067295-TAAG-T
• gnomAD v4: 18-51067295-TAAG-T
• MyVariant Identifiers: chr18:g.48593666_48593668del (hg19) ; chr18:g.51067296_51067298del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.51067298_51067300del , CM000680.2:g.51067298_51067300del	GRCh38
NC_000018.9:g.48593668_48593670del , CM000680.1:g.48593668_48593670del	GRCh37
NC_000018.8:g.46847666_46847668del	NCBI36
NG_013013.2:g.104259_104261del , LRG_318:g.104259_104261del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588860.6:c.1308+111_1308+113del	ENSP00000465878.2:n.1308+111_1308+113del
ENST00000589076.6:c.1308+111_1308+113del	ENSP00000466934.2:n.1308+111_1308+113del
ENST00000589941.2:c.1308+111_1308+113del	ENSP00000465874.2:n.1308+111_1308+113del
ENST00000590061.2:c.1308+111_1308+113del	ENSP00000464772.2:n.1308+111_1308+113del
ENST00000593223.2:c.1308+111_1308+113del	ENSP00000466118.2:n.1308+111_1308+113del
ENST00000611848.2:c.1308+111_1308+113del	ENSP00000478613.2:n.1308+111_1308+113del
ENST00000684953.1:n.2680+111_2680+113del
ENST00000685090.1:n.1759+111_1759+113del
ENST00000685232.1:n.1416+111_1416+113del
ENST00000688574.1:n.1416+111_1416+113del
ENST00000691124.1:n.2790+111_2790+113del
ENST00000342988.8:c.1308+111_1308+113del MANE Select	ENSP00000341551.3:n.1308+111_1308+113del
ENST00000342988.7:c.1308+111_1308+113del	ENSP00000341551.3:n.1308+111_1308+113del
ENST00000398417.6:c.1308+111_1308+113del	ENSP00000381452.1:n.1308+111_1308+113del
ENST00000588745.5:c.1020+111_1020+113del	ENSP00000464901.1:n.1020+111_1020+113del
ENST00000590499.1:n.366+111_366+113del
ENST00000591126.5:n.3309+111_3309+113del
ENST00000592186.5:c.955+7382_955+7384del	ENSP00000468611.1:n.955+7382_955+7384del
ENST00000593223.1:c.75+111_75+113del	ENSP00000466118.1:n.75+111_75+113del
ENST00000611848.1:c.508+111_508+113del
NM_005359.5:c.1308+111_1308+113del , LRG_318t1:c.1308+111_1308+113del	NP_005350.1:n.1308+111_1308+113del
NM_005359.6:c.1308+111_1308+113del MANE Select	NP_005350.1:n.1308+111_1308+113del