Canonical Allele Identifier: CA2302989931
Gene: SMAD4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.51084380G= , CM000680.2:g.51084380G= GRCh38
NC_000018.9:g.48610750G= , CM000680.1:g.48610750G= GRCh37
NC_000018.8:g.46864748G= NCBI36
NG_013013.2:g.121341G= , LRG_318:g.121341G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000588860.6:c.*5913G= ENSP00000465878.2:n.*5913G=
ENST00000589076.6:c.*5913G= ENSP00000466934.2:n.*5913G=
ENST00000589941.2:c.*5913G= ENSP00000465874.2:n.*5913G=
ENST00000590061.2:c.*5913G= ENSP00000464772.2:n.*5913G=
ENST00000688574.1:n.7680G=
ENST00000342988.8:c.*5913G= MANE Select ENSP00000341551.3:n.*5913G=
ENST00000342988.7:c.*5913G= ENSP00000341551.3:n.*5913G=
ENST00000398417.6:c.*5913G= ENSP00000381452.1:n.*5913G=
NM_005359.5:c.*5913G= , LRG_318t1:c.*5913G= NP_005350.1:n.*5913G=
NM_005359.6:c.*5913G= MANE Select NP_005350.1:n.*5913G=