Canonical Allele Identifier: CA2302989580
Gene: SMAD4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.51083965C= , CM000680.2:g.51083965C= GRCh38
NC_000018.9:g.48610335C= , CM000680.1:g.48610335C= GRCh37
NC_000018.8:g.46864333C= NCBI36
NG_013013.2:g.120926C= , LRG_318:g.120926C=

Transcript Alleles

HGVS Amino-acid change
ENST00000588860.6:c.*5498C= ENSP00000465878.2:n.*5498C=
ENST00000589076.6:c.*5498C= ENSP00000466934.2:n.*5498C=
ENST00000589941.2:c.*5498C= ENSP00000465874.2:n.*5498C=
ENST00000590061.2:c.*5498C= ENSP00000464772.2:n.*5498C=
ENST00000688574.1:n.7265C=
ENST00000342988.8:c.*5498C= MANE Select ENSP00000341551.3:n.*5498C=
ENST00000342988.7:c.*5498C= ENSP00000341551.3:n.*5498C=
ENST00000398417.6:c.*5498C= ENSP00000381452.1:n.*5498C=
NM_005359.5:c.*5498C= , LRG_318t1:c.*5498C= NP_005350.1:n.*5498C=
NM_005359.6:c.*5498C= MANE Select NP_005350.1:n.*5498C=