Canonical Allele Identifier: CA8965916
Gene: SMAD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 240155
dbSNP Id: rs370176106
COSMIC: COSM988904

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.51058436C>T , CM000680.2:g.51058436C>T GRCh38
NC_000018.9:g.48584806C>T , CM000680.1:g.48584806C>T GRCh37
NC_000018.8:g.46838804C>T NCBI36
NG_013013.2:g.95397C>T , LRG_318:g.95397C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000588860.6:c.884C>T ENSP00000465878.2:p.Pro295Leu
ENST00000589076.6:c.884C>T ENSP00000466934.2:p.Pro295Leu
ENST00000589941.2:c.884C>T ENSP00000465874.2:p.Pro295Leu
ENST00000590061.2:c.884C>T ENSP00000464772.2:p.Pro295Leu
ENST00000593223.2:c.884C>T ENSP00000466118.2:p.Pro295Leu
ENST00000611848.2:c.884C>T ENSP00000478613.2:p.Pro295Leu
ENST00000684953.1:n.2256C>T
ENST00000685232.1:n.992C>T
ENST00000688307.1:n.156-1430C>T
ENST00000688574.1:n.992C>T
ENST00000688903.1:n.1098C>T
ENST00000690892.1:n.992C>T
ENST00000342988.8:c.884C>T MANE Select ENSP00000341551.3:p.Pro295Leu
ENST00000342988.7:c.884C>T ENSP00000341551.3:p.Pro295Leu
ENST00000398417.6:c.884C>T ENSP00000381452.1:p.Pro295Leu
ENST00000588745.5:c.667+3443C>T ENSP00000464901.1:n.667+3443C>T
ENST00000591126.5:n.2885C>T
ENST00000592186.5:c.884C>T ENSP00000468611.1:p.Pro295Leu
ENST00000611848.1:c.84C>T
NM_005359.5:c.884C>T , LRG_318t1:c.884C>T NP_005350.1:p.Pro295Leu
NM_005359.6:c.884C>T MANE Select NP_005350.1:p.Pro295Leu