Canonical Allele Identifier: CA16620696

Gene: SMAD4

Linked Data

• ClinVar Variation Id: 422097
• ClinVar RCV Id: RCV000480335
• dbSNP Id: rs1064795555
• MyVariant Identifiers: chr18:g.48573364_48573369del (hg19) ; chr18:g.51046994_51046999del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.51046994_51046999del , CM000680.2:g.51046994_51046999del	GRCh38
NC_000018.9:g.48573364_48573369del , CM000680.1:g.48573364_48573369del	GRCh37
NC_000018.8:g.46827362_46827367del	NCBI36
NG_013013.2:g.83955_83960del , LRG_318:g.83955_83960del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588860.6:c.-53_-48del	ENSP00000465878.2:n.-53_-48del
ENST00000589076.6:c.-53_-48del	ENSP00000466934.2:n.-53_-48del
ENST00000589941.2:c.-53_-48del	ENSP00000465874.2:n.-53_-48del
ENST00000590061.2:c.-53_-48del	ENSP00000464772.2:n.-53_-48del
ENST00000593223.2:c.-53_-48del	ENSP00000466118.2:n.-53_-48del
ENST00000611848.2:c.-53_-48del	ENSP00000478613.2:n.-53_-48del
ENST00000342988.8:c.-53_-48del MANE Select	ENSP00000341551.3:n.-53_-48del
ENST00000342988.7:c.-53_-48del	ENSP00000341551.3:n.-53_-48del
ENST00000398417.6:c.-53_-48del	ENSP00000381452.1:n.-53_-48del
ENST00000588256.1:n.409_414del
ENST00000588860.5:c.-53_-48del	ENSP00000465878.1:n.-53_-48del
ENST00000589076.5:c.-53_-48del	ENSP00000466934.1:n.-53_-48del
ENST00000589941.1:c.-53_-48del	ENSP00000465874.1:n.-53_-48del
ENST00000590061.1:c.-53_-48del	ENSP00000464772.1:n.-53_-48del
ENST00000590722.2:c.232_237del	ENSP00000465737.1:p.Asn78_Cys79del
ENST00000591914.5:c.-53_-48del	ENSP00000466941.1:n.-53_-48del
ENST00000592911.5:n.28-1692_28-1687del
NM_005359.5:c.-53_-48del , LRG_318t1:c.-53_-48del	NP_005350.1:n.-53_-48del
NM_005359.6:c.-53_-48del MANE Select	NP_005350.1:n.-53_-48del