Canonical Allele Identifier: CA2184410880

Gene: SMAD3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.67165350C= , CM000677.2:g.67165350C=	GRCh38
NC_000015.9:g.67457688C= , CM000677.1:g.67457688C=	GRCh37
NC_000015.8:g.65244742C=	NCBI36
NG_011990.1:g.104494C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000558739.2:c.183C=	ENSP00000453684.2:p.Phe61=
ENST00000559460.6:c.183C=	ENSP00000453082.2:p.Phe61=
ENST00000560424.2:c.498C=	ENSP00000455540.2:p.Phe166=
ENST00000327367.9:c.498C= MANE Select	ENSP00000332973.4:p.Phe166=
ENST00000679624.1:c.183C=	ENSP00000505445.1:p.Phe61=
ENST00000681239.1:c.183C=	ENSP00000505641.1:p.Phe61=
ENST00000327367.8:c.498C=	ENSP00000332973.4:p.Phe166=
ENST00000439724.7:c.366C=	ENSP00000401133.3:p.Phe122=
ENST00000540846.6:c.183C=	ENSP00000437757.2:p.Phe61=
ENST00000558739.1:c.183C=	ENSP00000453684.1:p.Phe61=
ENST00000558894.5:c.183C=	ENSP00000458060.1:p.Phe61=
ENST00000559460.5:c.183C=	ENSP00000453082.1:p.Phe61=
ENST00000559937.1:n.348C=
ENST00000560175.5:c.183C=	ENSP00000455095.1:p.Phe61=
NM_001145102.1:c.183C=	NP_001138574.1:p.Phe61=
NM_001145103.1:c.366C=	NP_001138575.1:p.Phe122=
NM_005902.3:c.498C=	NP_005893.1:p.Phe166=
XM_011521559.1:c.400+262C=	XP_011519861.1:n.400+262C=
XM_011521560.1:c.351C=	XP_011519862.1:p.Phe117=
XM_011521559.3:c.400+262C=	XP_011519861.1:n.400+262C=
NM_005902.4:c.498C= MANE Select	NP_005893.1:p.Phe166=
NM_001145102.2:c.183C=	NP_001138574.1:p.Phe61=
NM_001145103.2:c.366C=	NP_001138575.1:p.Phe122=