Canonical Allele Identifier: CA990249180
Gene: SMAD4 HGNC NCBI

Linked Data

dbSNP Id: rs886053930

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.51084043C>T , CM000680.2:g.51084043C>T GRCh38
NC_000018.9:g.48610413C>T , CM000680.1:g.48610413C>T GRCh37
NC_000018.8:g.46864411C>T NCBI36
NG_013013.2:g.121004C>T , LRG_318:g.121004C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000588860.6:c.*5576C>T ENSP00000465878.2:n.*5576C>T
ENST00000589076.6:c.*5576C>T ENSP00000466934.2:n.*5576C>T
ENST00000589941.2:c.*5576C>T ENSP00000465874.2:n.*5576C>T
ENST00000590061.2:c.*5576C>T ENSP00000464772.2:n.*5576C>T
ENST00000688574.1:n.7343C>T
ENST00000342988.8:c.*5576C>T MANE Select ENSP00000341551.3:n.*5576C>T
ENST00000342988.7:c.*5576C>T ENSP00000341551.3:n.*5576C>T
ENST00000398417.6:c.*5576C>T ENSP00000381452.1:n.*5576C>T
NM_005359.5:c.*5576C>T , LRG_318t1:c.*5576C>T NP_005350.1:n.*5576C>T
NM_005359.6:c.*5576C>T MANE Select NP_005350.1:n.*5576C>T