Canonical Allele Identifier: CA2184394427
Gene: SMAD3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.67145434A= , CM000677.2:g.67145434A= GRCh38
NC_000015.9:g.67437772A= , CM000677.1:g.67437772A= GRCh37
NC_000015.8:g.65224826A= NCBI36
NG_011990.1:g.84578A=

Transcript Alleles

HGVS Amino-acid change
ENST00000558739.2:c.-110+6912A= ENSP00000453684.2:n.-110+6912A=
ENST00000559460.6:c.-109-19461A= ENSP00000453082.2:n.-109-19461A=
ENST00000560424.2:c.207-19461A= ENSP00000455540.2:n.207-19461A=
ENST00000327367.9:c.207-19461A= MANE Select ENSP00000332973.4:n.207-19461A=
ENST00000679624.1:c.-109-19461A= ENSP00000505445.1:n.-109-19461A=
ENST00000681239.1:c.-110+5712A= ENSP00000505641.1:n.-110+5712A=
ENST00000327367.8:c.207-19461A= ENSP00000332973.4:n.207-19461A=
ENST00000439724.7:c.74+7334A= ENSP00000401133.3:n.74+7334A=
ENST00000540846.6:c.-110+19450A= ENSP00000437757.2:n.-110+19450A=
ENST00000558739.1:c.-110+6912A= ENSP00000453684.1:n.-110+6912A=
ENST00000558894.5:c.-110+17283A= ENSP00000458060.1:n.-110+17283A=
ENST00000559092.1:c.152-19461A= ENSP00000453788.1:n.152-19461A=
ENST00000559460.5:c.-109-19461A= ENSP00000453082.1:n.-109-19461A=
ENST00000559937.1:n.57-19461A=
ENST00000560175.5:c.-109-19461A= ENSP00000455095.1:n.-109-19461A=
NM_001145102.1:c.-110+19450A= NP_001138574.1:n.-110+19450A=
NM_001145103.1:c.74+7334A= NP_001138575.1:n.74+7334A=
NM_005902.3:c.207-19461A= NP_005893.1:n.207-19461A=
XM_011521559.1:c.207-19461A= XP_011519861.1:n.207-19461A=
XM_011521560.1:c.60-19461A= XP_011519862.1:n.60-19461A=
XM_011521559.3:c.207-19461A= XP_011519861.1:n.207-19461A=
NM_005902.4:c.207-19461A= MANE Select NP_005893.1:n.207-19461A=
NM_001145102.2:c.-110+19450A= NP_001138574.1:n.-110+19450A=
NM_001145103.2:c.74+7334A= NP_001138575.1:n.74+7334A=