Canonical Allele Identifier: CA13909711

Gene: SMAD9

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.36872574G>T , CM000675.2:g.36872574G>T	GRCh38
NC_000013.10:g.37446711G>T , CM000675.1:g.37446711G>T	GRCh37
NC_000013.9:g.36344711G>T	NCBI36
NG_016963.1:g.52699C>A , LRG_703:g.52699C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001127217.3:c.670+84C>A MANE Select	NP_001120689.1:n.670+84C>A
ENST00000379826.5:c.670+84C>A MANE Select	ENSP00000369154.4:n.670+84C>A
NM_001127217.2:c.670+84C>A , LRG_703t1:c.670+84C>A	NP_001120689.1:n.670+84C>A
NM_001378621.1:c.670+84C>A	NP_001365550.1:n.670+84C>A
NM_005905.5:c.670+84C>A	NP_005896.1:n.670+84C>A
NM_005905.6:c.670+84C>A	NP_005896.1:n.670+84C>A
ENST00000350148.10:c.670+84C>A	ENSP00000239885.6:n.670+84C>A
ENST00000350148.9:c.670+84C>A	ENSP00000239885.6:n.670+84C>A
ENST00000379826.4:c.670+84C>A	ENSP00000369154.4:n.670+84C>A
ENST00000399275.6:c.670+84C>A	ENSP00000382216.2:n.670+84C>A
ENST00000399275.7:c.*380+84C>A	ENSP00000382216.3:n.*380+84C>A
XM_005266401.2:c.670+84C>A	XP_005266458.1:n.670+84C>A
XM_005266401.3:c.670+84C>A	XP_005266458.1:n.670+84C>A
XM_005266403.2:c.413-5191C>A	XP_005266460.1:n.413-5191C>A
XM_005266403.3:c.413-5191C>A	XP_005266460.1:n.413-5191C>A
XM_005266404.2:c.412+6704C>A	XP_005266461.1:n.412+6704C>A
XM_005266404.3:c.412+6704C>A	XP_005266461.1:n.412+6704C>A
XM_006719827.2:c.670+84C>A	XP_006719890.1:n.670+84C>A
XM_006719827.3:c.670+84C>A	XP_006719890.1:n.670+84C>A
XM_011535096.1:c.670+84C>A	XP_011533398.1:n.670+84C>A