Canonical Allele Identifier: CA2184395609

Gene: SMAD3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.67146869T= , CM000677.2:g.67146869T=	GRCh38
NC_000015.9:g.67439207T= , CM000677.1:g.67439207T=	GRCh37
NC_000015.8:g.65226261T=	NCBI36
NG_011990.1:g.86013T=

Transcript Alleles

HGVS	Amino-acid Change
NM_005902.4:c.207-18026T= MANE Select	NP_005893.1:n.207-18026T=
ENST00000327367.9:c.207-18026T= MANE Select	ENSP00000332973.4:n.207-18026T=
NM_001145102.1:c.-109-18026T=	NP_001138574.1:n.-109-18026T=
NM_001145102.2:c.-109-18026T=	NP_001138574.1:n.-109-18026T=
NM_001145103.1:c.74+8769T=	NP_001138575.1:n.74+8769T=
NM_001145103.2:c.74+8769T=	NP_001138575.1:n.74+8769T=
NM_005902.3:c.207-18026T=	NP_005893.1:n.207-18026T=
ENST00000327367.8:c.207-18026T=	ENSP00000332973.4:n.207-18026T=
ENST00000439724.7:c.74+8769T=	ENSP00000401133.3:n.74+8769T=
ENST00000540846.6:c.-109-18026T=	ENSP00000437757.2:n.-109-18026T=
ENST00000558739.1:c.-110+8347T=	ENSP00000453684.1:n.-110+8347T=
ENST00000558739.2:c.-110+8347T=	ENSP00000453684.2:n.-110+8347T=
ENST00000558894.5:c.-109-18026T=	ENSP00000458060.1:n.-109-18026T=
ENST00000559092.1:c.152-18026T=	ENSP00000453788.1:n.152-18026T=
ENST00000559460.5:c.-109-18026T=	ENSP00000453082.1:n.-109-18026T=
ENST00000559460.6:c.-109-18026T=	ENSP00000453082.2:n.-109-18026T=
ENST00000559937.1:n.57-18026T=
ENST00000560175.5:c.-109-18026T=	ENSP00000455095.1:n.-109-18026T=
ENST00000560424.2:c.207-18026T=	ENSP00000455540.2:n.207-18026T=
ENST00000679624.1:c.-109-18026T=	ENSP00000505445.1:n.-109-18026T=
ENST00000681239.1:c.-110+7147T=	ENSP00000505641.1:n.-110+7147T=
XM_011521559.1:c.207-18026T=	XP_011519861.1:n.207-18026T=
XM_011521559.3:c.207-18026T=	XP_011519861.1:n.207-18026T=
XM_011521560.1:c.60-18026T=	XP_011519862.1:n.60-18026T=