Canonical Allele Identifier: CA402465818

Gene: SMAD4

Linked Data

• ClinVar Variation Id: 2882926
• ClinVar RCV Id: RCV003763558
• MyVariant Identifiers: chr18:g.48604676A>C (hg19) ; chr18:g.51078306A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.51078306A>C , CM000680.2:g.51078306A>C	GRCh38
NC_000018.9:g.48604676A>C , CM000680.1:g.48604676A>C	GRCh37
NC_000018.8:g.46858674A>C	NCBI36
NG_013013.2:g.115267A>C , LRG_318:g.115267A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588860.6:c.1498A>C	ENSP00000465878.2:p.Ile500Leu
ENST00000589076.6:c.1498A>C	ENSP00000466934.2:p.Ile500Leu
ENST00000589941.2:c.1498A>C	ENSP00000465874.2:p.Ile500Leu
ENST00000590061.2:c.1498A>C	ENSP00000464772.2:p.Ile500Leu
ENST00000593223.2:c.*1495A>C	ENSP00000466118.2:n.*1495A>C
ENST00000611848.2:c.*150A>C	ENSP00000478613.2:n.*150A>C
ENST00000684953.1:n.3513A>C
ENST00000685090.1:n.3428A>C
ENST00000685232.1:n.1719A>C
ENST00000688574.1:n.1606A>C
ENST00000691124.1:n.4459A>C
ENST00000342988.8:c.1498A>C MANE Select	ENSP00000341551.3:p.Ile500Leu
ENST00000342988.7:c.1498A>C	ENSP00000341551.3:p.Ile500Leu
ENST00000398417.6:c.1498A>C	ENSP00000381452.1:p.Ile500Leu
ENST00000586253.1:n.220A>C
ENST00000588745.5:c.1210A>C	ENSP00000464901.1:p.Ile404Leu
ENST00000591126.5:n.3499A>C
ENST00000592186.5:c.1145A>C	ENSP00000468611.1:n.1145A>C
ENST00000611848.1:c.811A>C
NM_005359.5:c.1498A>C , LRG_318t1:c.1498A>C	NP_005350.1:p.Ile500Leu
NM_005359.6:c.1498A>C MANE Select	NP_005350.1:p.Ile500Leu