Canonical Allele Identifier: CA503993792

Gene: SMAD4

Linked Data

• ClinVar Variation Id: 1618666
• ClinVar RCV Id: RCV002094072
• dbSNP Id: rs2144426653
• MyVariant Identifiers: chr18:g.48584502T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.51058132T>G , CM000680.2:g.51058132T>G	GRCh38
NC_000018.9:g.48584502T>G , CM000680.1:g.48584502T>G	GRCh37
NC_000018.8:g.46838500T>G	NCBI36
NG_013013.2:g.95093T>G , LRG_318:g.95093T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000588860.6:c.675T>G	ENSP00000465878.2:p.Pro225=
ENST00000589076.6:c.675T>G	ENSP00000466934.2:p.Pro225=
ENST00000589941.2:c.675T>G	ENSP00000465874.2:p.Pro225=
ENST00000590061.2:c.675T>G	ENSP00000464772.2:p.Pro225=
ENST00000593223.2:c.675T>G	ENSP00000466118.2:p.Pro225=
ENST00000611848.2:c.675T>G	ENSP00000478613.2:p.Pro225=
ENST00000684953.1:n.2047T>G
ENST00000685232.1:n.783T>G
ENST00000688307.1:n.156-1734T>G
ENST00000688574.1:n.783T>G
ENST00000688903.1:n.889T>G
ENST00000690892.1:n.783T>G
ENST00000342988.8:c.675T>G MANE Select	ENSP00000341551.3:p.Pro225=
ENST00000342988.7:c.675T>G	ENSP00000341551.3:p.Pro225=
ENST00000398417.6:c.675T>G	ENSP00000381452.1:p.Pro225=
ENST00000588745.5:c.667+3139T>G	ENSP00000464901.1:n.667+3139T>G
ENST00000590722.2:c.*851T>G	ENSP00000465737.1:n.*851T>G
ENST00000591126.5:n.2676T>G
ENST00000592186.5:c.675T>G	ENSP00000468611.1:p.Pro225=
ENST00000592911.5:n.453T>G
NM_005359.5:c.675T>G , LRG_318t1:c.675T>G	NP_005350.1:p.Pro225=
NM_005359.6:c.675T>G MANE Select	NP_005350.1:p.Pro225=