Canonical Allele Identifier: CA2302977031
Gene: SMAD4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.51058040G= , CM000680.2:g.51058040G= GRCh38
NC_000018.9:g.48584410G= , CM000680.1:g.48584410G= GRCh37
NC_000018.8:g.46838408G= NCBI36
NG_013013.2:g.95001G= , LRG_318:g.95001G=

Transcript Alleles

HGVS Amino-acid change
ENST00000588860.6:c.668-85G= ENSP00000465878.2:n.668-85G=
ENST00000589076.6:c.668-85G= ENSP00000466934.2:n.668-85G=
ENST00000589941.2:c.668-85G= ENSP00000465874.2:n.668-85G=
ENST00000590061.2:c.668-85G= ENSP00000464772.2:n.668-85G=
ENST00000593223.2:c.668-85G= ENSP00000466118.2:n.668-85G=
ENST00000611848.2:c.668-85G= ENSP00000478613.2:n.668-85G=
ENST00000684953.1:n.2040-85G=
ENST00000685232.1:n.691G=
ENST00000688307.1:n.156-1826G=
ENST00000688574.1:n.691G=
ENST00000688903.1:n.797G=
ENST00000690892.1:n.691G=
ENST00000342988.8:c.668-85G= MANE Select ENSP00000341551.3:n.668-85G=
ENST00000342988.7:c.668-85G= ENSP00000341551.3:n.668-85G=
ENST00000398417.6:c.668-85G= ENSP00000381452.1:n.668-85G=
ENST00000588745.5:c.667+3047G= ENSP00000464901.1:n.667+3047G=
ENST00000590722.2:c.*844-85G= ENSP00000465737.1:n.*844-85G=
ENST00000591126.5:n.2669-85G=
ENST00000592186.5:c.668-85G= ENSP00000468611.1:n.668-85G=
ENST00000592911.5:n.446-85G=
NM_005359.5:c.668-85G= , LRG_318t1:c.668-85G= NP_005350.1:n.668-85G=
NM_005359.6:c.668-85G= MANE Select NP_005350.1:n.668-85G=