Canonical Allele Identifier: CA402465423
Community Standard Title: NM_005359.6(SMAD4):c.1447+15C>A
Gene: SMAD4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.51076791C>A , CM000680.2:g.51076791C>A GRCh38
NC_000018.9:g.48603161C>A , CM000680.1:g.48603161C>A GRCh37
NC_000018.8:g.46857159C>A NCBI36
NG_013013.2:g.113752C>A , LRG_318:g.113752C>A

Transcript Alleles

HGVS Amino-acid Change
NM_005359.6:c.1447+15C>A MANE Select NP_005350.1:n.1447+15C>A
ENST00000342988.8:c.1447+15C>A MANE Select ENSP00000341551.3:n.1447+15C>A
NM_005359.5:c.1447+15C>A , LRG_318t1:c.1447+15C>A NP_005350.1:n.1447+15C>A
ENST00000342988.7:c.1447+15C>A ENSP00000341551.3:n.1447+15C>A
ENST00000398417.6:c.1447+15C>A ENSP00000381452.1:n.1447+15C>A
ENST00000588745.5:c.1159+15C>A ENSP00000464901.1:n.1159+15C>A
ENST00000588860.6:c.1447+15C>A ENSP00000465878.2:n.1447+15C>A
ENST00000589076.6:c.1447+15C>A ENSP00000466934.2:n.1447+15C>A
ENST00000589941.2:c.1447+15C>A ENSP00000465874.2:n.1447+15C>A
ENST00000590061.2:c.1447+15C>A ENSP00000464772.2:n.1447+15C>A
ENST00000590499.1:n.505+15C>A
ENST00000591126.5:n.3448+15C>A
ENST00000592186.5:c.1094+15C>A ENSP00000468611.1:n.1094+15C>A
ENST00000593223.1:c.229C>A ENSP00000466118.1:p.His77Asn
ENST00000593223.2:c.1462C>A ENSP00000466118.2:p.His488Asn
ENST00000611848.1:c.647+15C>A
ENST00000611848.2:c.1447+15C>A ENSP00000478613.2:n.1447+15C>A
ENST00000684953.1:n.2834C>A
ENST00000685090.1:n.1913C>A
ENST00000685232.1:n.1555+15C>A
ENST00000688574.1:n.1555+15C>A
ENST00000691124.1:n.2944C>A