Canonical Allele Identifier: CA2184369313
Gene: SMAD3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.67066329A= , CM000677.2:g.67066329A= GRCh38
NC_000015.9:g.67358667A= , CM000677.1:g.67358667A= GRCh37
NC_000015.8:g.65145721A= NCBI36
NG_011990.1:g.5473A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559460.6:c.-110+2385A= ENSP00000453082.2:n.-110+2385A=
ENST00000560424.2:c.175A= ENSP00000455540.2:p.Asn59=
ENST00000327367.9:c.175A= MANE Select ENSP00000332973.4:p.Asn59=
ENST00000327367.8:c.175A= ENSP00000332973.4:p.Asn59=
ENST00000559460.5:c.-110+2385A= ENSP00000453082.1:n.-110+2385A=
NM_005902.3:c.175A= NP_005893.1:p.Asn59=
XM_011521559.1:c.175A= XP_011519861.1:p.Asn59=
XM_011521559.3:c.175A= XP_011519861.1:p.Asn59=
NM_005902.4:c.175A= MANE Select NP_005893.1:p.Asn59=