Canonical Allele Identifier: CA2629114970
Gene: SMAD3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.67066367del , CM000677.2:g.67066367del GRCh38
NC_000015.9:g.67358705del , CM000677.1:g.67358705del GRCh37
NC_000015.8:g.65145759del NCBI36
NG_011990.1:g.5511del

Transcript Alleles

HGVS Amino-acid Change
ENST00000559460.6:c.-110+2423del ENSP00000453082.2:n.-110+2423del
ENST00000560424.2:c.206+7del ENSP00000455540.2:n.206+7del
ENST00000327367.9:c.206+7del MANE Select ENSP00000332973.4:n.206+7del
ENST00000327367.8:c.206+7del ENSP00000332973.4:n.206+7del
ENST00000559460.5:c.-110+2423del ENSP00000453082.1:n.-110+2423del
NM_005902.3:c.206+7del NP_005893.1:n.206+7del
XM_011521559.1:c.206+7del XP_011519861.1:n.206+7del
XM_011521559.3:c.206+7del XP_011519861.1:n.206+7del
NM_005902.4:c.206+7del MANE Select NP_005893.1:n.206+7del