Canonical Allele Identifier: CA16620697

Gene: SMAD4

Linked Data

• ClinVar Variation Id: 422433
• ClinVar RCV Id: RCV000481044 ; RCV001865469
• dbSNP Id: rs1064795777
• MyVariant Identifiers: chr18:g.48573417A>G (hg19) ; chr18:g.51047047A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.51047047A>G , CM000680.2:g.51047047A>G	GRCh38
NC_000018.9:g.48573417A>G , CM000680.1:g.48573417A>G	GRCh37
NC_000018.8:g.46827415A>G	NCBI36
NG_013013.2:g.84008A>G , LRG_318:g.84008A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588860.6:c.1A>G	ENSP00000465878.2:p.Met1Val
ENST00000589076.6:c.1A>G	ENSP00000466934.2:p.Met1Val
ENST00000589941.2:c.1A>G	ENSP00000465874.2:p.Met1Val
ENST00000590061.2:c.1A>G	ENSP00000464772.2:p.Met1Val
ENST00000593223.2:c.1A>G	ENSP00000466118.2:p.Met1Val
ENST00000611848.2:c.1A>G	ENSP00000478613.2:p.Met1Val
ENST00000342988.8:c.1A>G MANE Select	ENSP00000341551.3:p.Met1Val
ENST00000342988.7:c.1A>G	ENSP00000341551.3:p.Met1Val
ENST00000398417.6:c.1A>G	ENSP00000381452.1:p.Met1Val
ENST00000588256.1:n.462A>G
ENST00000588745.5:c.1A>G	ENSP00000464901.1:p.Met1Val
ENST00000588860.5:c.1A>G	ENSP00000465878.1:p.Met1Val
ENST00000589076.5:c.1A>G	ENSP00000466934.1:p.Met1Val
ENST00000589941.1:c.1A>G	ENSP00000465874.1:p.Met1Val
ENST00000590061.1:c.1A>G	ENSP00000464772.1:p.Met1Val
ENST00000590722.2:c.*24A>G	ENSP00000465737.1:n.*24A>G
ENST00000591914.5:c.1A>G	ENSP00000466941.1:p.Met1Val
ENST00000592186.5:c.1A>G	ENSP00000468611.1:p.Met1Val
ENST00000592911.5:n.28-1639A>G
NM_005359.5:c.1A>G , LRG_318t1:c.1A>G	NP_005350.1:p.Met1Val
NM_005359.6:c.1A>G MANE Select	NP_005350.1:p.Met1Val