Canonical Allele Identifier: CA16607982

Gene: SMAD4

Linked Data

• ClinVar Variation Id: 390388
• ClinVar RCV Id: RCV000440329 ; RCV000767314
• dbSNP Id: rs1057523754
• MyVariant Identifiers: chr18:g.48573378T>A (hg19) ; chr18:g.51047008T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.51047008T>A , CM000680.2:g.51047008T>A	GRCh38
NC_000018.9:g.48573378T>A , CM000680.1:g.48573378T>A	GRCh37
NC_000018.8:g.46827376T>A	NCBI36
NG_013013.2:g.83969T>A , LRG_318:g.83969T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588860.6:c.-39T>A	ENSP00000465878.2:n.-39T>A
ENST00000589076.6:c.-39T>A	ENSP00000466934.2:n.-39T>A
ENST00000589941.2:c.-39T>A	ENSP00000465874.2:n.-39T>A
ENST00000590061.2:c.-39T>A	ENSP00000464772.2:n.-39T>A
ENST00000593223.2:c.-39T>A	ENSP00000466118.2:n.-39T>A
ENST00000611848.2:c.-39T>A	ENSP00000478613.2:n.-39T>A
ENST00000342988.8:c.-39T>A MANE Select	ENSP00000341551.3:n.-39T>A
ENST00000342988.7:c.-39T>A	ENSP00000341551.3:n.-39T>A
ENST00000398417.6:c.-39T>A	ENSP00000381452.1:n.-39T>A
ENST00000588256.1:n.423T>A
ENST00000588860.5:c.-39T>A	ENSP00000465878.1:n.-39T>A
ENST00000589076.5:c.-39T>A	ENSP00000466934.1:n.-39T>A
ENST00000589941.1:c.-39T>A	ENSP00000465874.1:n.-39T>A
ENST00000590061.1:c.-39T>A	ENSP00000464772.1:n.-39T>A
ENST00000590722.2:c.246T>A	ENSP00000465737.1:p.Asn82Lys
ENST00000591914.5:c.-39T>A	ENSP00000466941.1:n.-39T>A
ENST00000592911.5:n.28-1678T>A
NM_005359.5:c.-39T>A , LRG_318t1:c.-39T>A	NP_005350.1:n.-39T>A
NM_005359.6:c.-39T>A MANE Select	NP_005350.1:n.-39T>A