Canonical Allele Identifier: CA387852959

Gene: SMAD9

Linked Data

• MyVariant Identifiers: chr13:g.37453621A>T (hg19) ; chr13:g.36879484A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.36879484A>T , CM000675.2:g.36879484A>T	GRCh38
NC_000013.10:g.37453621A>T , CM000675.1:g.37453621A>T	GRCh37
NC_000013.9:g.36351621A>T	NCBI36
NG_016963.1:g.45789T>A , LRG_703:g.45789T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000483941.2:n.645T>A
ENST00000350148.10:c.206T>A	ENSP00000239885.6:p.Val69Asp
ENST00000379826.5:c.206T>A MANE Select	ENSP00000369154.4:p.Val69Asp
ENST00000399275.7:c.206T>A	ENSP00000382216.3:p.Val69Asp
ENST00000350148.9:c.206T>A	ENSP00000239885.6:p.Val69Asp
ENST00000379826.4:c.206T>A	ENSP00000369154.4:p.Val69Asp
ENST00000399275.6:c.206T>A	ENSP00000382216.2:p.Val69Asp
ENST00000483941.1:n.523T>A
NM_001127217.2:c.206T>A , LRG_703t1:c.206T>A	NP_001120689.1:p.Val69Asp
NM_005905.5:c.206T>A	NP_005896.1:p.Val69Asp
XM_005266401.2:c.206T>A	XP_005266458.1:p.Val69Asp
XM_005266403.2:c.206T>A	XP_005266460.1:p.Val69Asp
XM_005266404.2:c.206T>A	XP_005266461.1:p.Val69Asp
XM_006719827.2:c.206T>A	XP_006719890.1:p.Val69Asp
XM_011535096.1:c.206T>A	XP_011533398.1:p.Val69Asp
XM_005266401.3:c.206T>A	XP_005266458.1:p.Val69Asp
XM_005266403.3:c.206T>A	XP_005266460.1:p.Val69Asp
XM_005266404.3:c.206T>A	XP_005266461.1:p.Val69Asp
XM_006719827.3:c.206T>A	XP_006719890.1:p.Val69Asp
NM_001127217.3:c.206T>A MANE Select	NP_001120689.1:p.Val69Asp
NM_005905.6:c.206T>A	NP_005896.1:p.Val69Asp
NM_001378621.1:c.206T>A	NP_001365550.1:p.Val69Asp