Canonical Allele Identifier: CA2739268754

Gene: SMAD4

Linked Data

• ClinVar Variation Id: 2908114
• ClinVar RCV Id: RCV003764351

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.51065409T>C , CM000680.2:g.51065409T>C	GRCh38
NC_000018.9:g.48591779T>C , CM000680.1:g.48591779T>C	GRCh37
NC_000018.8:g.46845777T>C	NCBI36
NG_013013.2:g.102370T>C , LRG_318:g.102370T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000588860.6:c.956-14T>C	ENSP00000465878.2:n.956-14T>C
ENST00000589076.6:c.956-14T>C	ENSP00000466934.2:n.956-14T>C
ENST00000589941.2:c.956-14T>C	ENSP00000465874.2:n.956-14T>C
ENST00000590061.2:c.956-14T>C	ENSP00000464772.2:n.956-14T>C
ENST00000593223.2:c.956-14T>C	ENSP00000466118.2:n.956-14T>C
ENST00000611848.2:c.956-14T>C	ENSP00000478613.2:n.956-14T>C
ENST00000684953.1:n.2328-14T>C
ENST00000685090.1:n.1407-14T>C
ENST00000685232.1:n.1064-14T>C
ENST00000688307.1:n.207-14T>C
ENST00000688574.1:n.1064-14T>C
ENST00000688903.1:n.1170-14T>C
ENST00000691124.1:n.2424T>C
ENST00000342988.8:c.956-14T>C MANE Select	ENSP00000341551.3:n.956-14T>C
ENST00000342988.7:c.956-14T>C	ENSP00000341551.3:n.956-14T>C
ENST00000398417.6:c.956-14T>C	ENSP00000381452.1:n.956-14T>C
ENST00000588745.5:c.668-14T>C	ENSP00000464901.1:n.668-14T>C
ENST00000591126.5:n.2957-14T>C
ENST00000592186.5:c.955+5493T>C	ENSP00000468611.1:n.955+5493T>C
ENST00000611848.1:c.156-14T>C
NM_005359.5:c.956-14T>C , LRG_318t1:c.956-14T>C	NP_005350.1:n.956-14T>C
NM_005359.6:c.956-14T>C MANE Select	NP_005350.1:n.956-14T>C