Canonical Allele Identifier: CA2184368437
Gene: SMAD3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.67065869_67065871delinsTCC , CM000677.2:g.67065869_67065871delinsTCC GRCh38
NC_000015.9:g.67358207_67358209delinsTCC , CM000677.1:g.67358207_67358209delinsTCC GRCh37
NC_000015.8:g.65145261_65145263delinsTCC NCBI36
NG_011990.1:g.5013_5015delinsTCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000559460.6:c.-110+1925_-110+1927delinsTCC ENSP00000453082.2:n.-110+1925_-110+1927delinsTCC
ENST00000560424.2:c.-286_-284delinsTCC ENSP00000455540.2:n.-286_-284delinsTCC
ENST00000327367.9:c.-286_-284delinsTCC MANE Select ENSP00000332973.4:n.-286_-284delinsTCC
ENST00000327367.8:c.-286_-284delinsTCC ENSP00000332973.4:n.-286_-284delinsTCC
ENST00000559460.5:c.-110+1925_-110+1927delinsTCC ENSP00000453082.1:n.-110+1925_-110+1927delinsTCC
NM_005902.3:c.-286_-284delinsTCC NP_005893.1:n.-286_-284delinsTCC
XM_011521559.1:c.-286_-284delinsTCC XP_011519861.1:n.-286_-284delinsTCC
NM_005902.4:c.-286_-284delinsTCC MANE Select NP_005893.1:n.-286_-284delinsTCC