Canonical Allele Identifier: CA2302989901
Gene: SMAD4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.51084301T= , CM000680.2:g.51084301T= GRCh38
NC_000018.9:g.48610671T= , CM000680.1:g.48610671T= GRCh37
NC_000018.8:g.46864669T= NCBI36
NG_013013.2:g.121262T= , LRG_318:g.121262T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000588860.6:c.*5834T= ENSP00000465878.2:n.*5834T=
ENST00000589076.6:c.*5834T= ENSP00000466934.2:n.*5834T=
ENST00000589941.2:c.*5834T= ENSP00000465874.2:n.*5834T=
ENST00000590061.2:c.*5834T= ENSP00000464772.2:n.*5834T=
ENST00000688574.1:n.7601T=
ENST00000342988.8:c.*5834T= MANE Select ENSP00000341551.3:n.*5834T=
ENST00000342988.7:c.*5834T= ENSP00000341551.3:n.*5834T=
ENST00000398417.6:c.*5834T= ENSP00000381452.1:n.*5834T=
NM_005359.5:c.*5834T= , LRG_318t1:c.*5834T= NP_005350.1:n.*5834T=
NM_005359.6:c.*5834T= MANE Select NP_005350.1:n.*5834T=