Canonical Allele Identifier: CA2184410479
Gene: SMAD3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.67165180T= , CM000677.2:g.67165180T= GRCh38
NC_000015.9:g.67457518T= , CM000677.1:g.67457518T= GRCh37
NC_000015.8:g.65244572T= NCBI36
NG_011990.1:g.104324T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000558739.2:c.86-73T= ENSP00000453684.2:n.86-73T=
ENST00000559460.6:c.86-73T= ENSP00000453082.2:n.86-73T=
ENST00000560424.2:c.401-73T= ENSP00000455540.2:n.401-73T=
ENST00000327367.9:c.401-73T= MANE Select ENSP00000332973.4:n.401-73T=
ENST00000679624.1:c.86-73T= ENSP00000505445.1:n.86-73T=
ENST00000681239.1:c.86-73T= ENSP00000505641.1:n.86-73T=
ENST00000327367.8:c.401-73T= ENSP00000332973.4:n.401-73T=
ENST00000439724.7:c.269-73T= ENSP00000401133.3:n.269-73T=
ENST00000540846.6:c.86-73T= ENSP00000437757.2:n.86-73T=
ENST00000558739.1:c.86-73T= ENSP00000453684.1:n.86-73T=
ENST00000558894.5:c.86-73T= ENSP00000458060.1:n.86-73T=
ENST00000559460.5:c.86-73T= ENSP00000453082.1:n.86-73T=
ENST00000559937.1:n.251-73T=
ENST00000560175.5:c.86-73T= ENSP00000455095.1:n.86-73T=
NM_001145102.1:c.86-73T= NP_001138574.1:n.86-73T=
NM_001145103.1:c.269-73T= NP_001138575.1:n.269-73T=
NM_005902.3:c.401-73T= NP_005893.1:n.401-73T=
XM_011521559.1:c.400+92T= XP_011519861.1:n.400+92T=
XM_011521560.1:c.254-73T= XP_011519862.1:n.254-73T=
XM_011521559.3:c.400+92T= XP_011519861.1:n.400+92T=
NM_005902.4:c.401-73T= MANE Select NP_005893.1:n.401-73T=
NM_001145102.2:c.86-73T= NP_001138574.1:n.86-73T=
NM_001145103.2:c.269-73T= NP_001138575.1:n.269-73T=