Canonical Allele Identifier: CA2629118119

Gene: SMAD3

Linked Data

• gnomAD v4: 15-67166307-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.67166307C>G , CM000677.2:g.67166307C>G	GRCh38
NC_000015.9:g.67458645C>G , CM000677.1:g.67458645C>G	GRCh37
NC_000015.8:g.65245699C>G	NCBI36
NG_011990.1:g.105451C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000558739.2:c.218-472C>G	ENSP00000453684.2:n.218-472C>G
ENST00000559460.6:c.218-472C>G	ENSP00000453082.2:n.218-472C>G
ENST00000560424.2:c.533-472C>G	ENSP00000455540.2:n.533-472C>G
ENST00000327367.9:c.533-472C>G MANE Select	ENSP00000332973.4:n.533-472C>G
ENST00000679624.1:c.218-472C>G	ENSP00000505445.1:n.218-472C>G
ENST00000681239.1:c.218-472C>G	ENSP00000505641.1:n.218-472C>G
ENST00000327367.8:c.533-472C>G	ENSP00000332973.4:n.533-472C>G
ENST00000439724.7:c.401-472C>G	ENSP00000401133.3:n.401-472C>G
ENST00000537194.6:c.-54+114C>G	ENSP00000445348.2:n.-54+114C>G
ENST00000540846.6:c.218-472C>G	ENSP00000437757.2:n.218-472C>G
ENST00000558894.5:c.218-472C>G	ENSP00000458060.1:n.218-472C>G
ENST00000559460.5:c.218-472C>G	ENSP00000453082.1:n.218-472C>G
ENST00000559937.1:n.383-472C>G
ENST00000560175.5:c.218-472C>G	ENSP00000455095.1:n.218-472C>G
NM_001145102.1:c.218-472C>G	NP_001138574.1:n.218-472C>G
NM_001145103.1:c.401-472C>G	NP_001138575.1:n.401-472C>G
NM_001145104.1:c.-54+114C>G	NP_001138576.1:n.-54+114C>G
NM_005902.3:c.533-472C>G	NP_005893.1:n.533-472C>G
XM_011521559.1:c.401-472C>G	XP_011519861.1:n.401-472C>G
XM_011521560.1:c.386-472C>G	XP_011519862.1:n.386-472C>G
XM_011521559.3:c.401-472C>G	XP_011519861.1:n.401-472C>G
NM_005902.4:c.533-472C>G MANE Select	NP_005893.1:n.533-472C>G
NM_001145102.2:c.218-472C>G	NP_001138574.1:n.218-472C>G
NM_001145103.2:c.401-472C>G	NP_001138575.1:n.401-472C>G
NM_001145104.2:c.-54+114C>G	NP_001138576.1:n.-54+114C>G