Canonical Allele Identifier: CA2184410814
Gene: SMAD3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.67165329C= , CM000677.2:g.67165329C= GRCh38
NC_000015.9:g.67457667C= , CM000677.1:g.67457667C= GRCh37
NC_000015.8:g.65244721C= NCBI36
NG_011990.1:g.104473C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000558739.2:c.162C= ENSP00000453684.2:p.Ser54=
ENST00000559460.6:c.162C= ENSP00000453082.2:p.Ser54=
ENST00000560424.2:c.477C= ENSP00000455540.2:p.Ser159=
ENST00000327367.9:c.477C= MANE Select ENSP00000332973.4:p.Ser159=
ENST00000679624.1:c.162C= ENSP00000505445.1:p.Ser54=
ENST00000681239.1:c.162C= ENSP00000505641.1:p.Ser54=
ENST00000327367.8:c.477C= ENSP00000332973.4:p.Ser159=
ENST00000439724.7:c.345C= ENSP00000401133.3:p.Ser115=
ENST00000540846.6:c.162C= ENSP00000437757.2:p.Ser54=
ENST00000558739.1:c.162C= ENSP00000453684.1:p.Ser54=
ENST00000558894.5:c.162C= ENSP00000458060.1:p.Ser54=
ENST00000559460.5:c.162C= ENSP00000453082.1:p.Ser54=
ENST00000559937.1:n.327C=
ENST00000560175.5:c.162C= ENSP00000455095.1:p.Ser54=
NM_001145102.1:c.162C= NP_001138574.1:p.Ser54=
NM_001145103.1:c.345C= NP_001138575.1:p.Ser115=
NM_005902.3:c.477C= NP_005893.1:p.Ser159=
XM_011521559.1:c.400+241C= XP_011519861.1:n.400+241C=
XM_011521560.1:c.330C= XP_011519862.1:p.Ser110=
XM_011521559.3:c.400+241C= XP_011519861.1:n.400+241C=
NM_005902.4:c.477C= MANE Select NP_005893.1:p.Ser159=
NM_001145102.2:c.162C= NP_001138574.1:p.Ser54=
NM_001145103.2:c.345C= NP_001138575.1:p.Ser115=