Canonical Allele Identifier: CA387853640

Gene: SMAD9

Linked Data

• MyVariant Identifiers: chr13:g.37453702A>C (hg19) ; chr13:g.36879565A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.36879565A>C , CM000675.2:g.36879565A>C	GRCh38
NC_000013.10:g.37453702A>C , CM000675.1:g.37453702A>C	GRCh37
NC_000013.9:g.36351702A>C	NCBI36
NG_016963.1:g.45708T>G , LRG_703:g.45708T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000483941.2:n.564T>G
ENST00000350148.10:c.125T>G	ENSP00000239885.6:p.Val42Gly
ENST00000379826.5:c.125T>G MANE Select	ENSP00000369154.4:p.Val42Gly
ENST00000399275.7:c.125T>G	ENSP00000382216.3:p.Val42Gly
ENST00000350148.9:c.125T>G	ENSP00000239885.6:p.Val42Gly
ENST00000379826.4:c.125T>G	ENSP00000369154.4:p.Val42Gly
ENST00000399275.6:c.125T>G	ENSP00000382216.2:p.Val42Gly
ENST00000483941.1:n.442T>G
NM_001127217.2:c.125T>G , LRG_703t1:c.125T>G	NP_001120689.1:p.Val42Gly
NM_005905.5:c.125T>G	NP_005896.1:p.Val42Gly
XM_005266401.2:c.125T>G	XP_005266458.1:p.Val42Gly
XM_005266403.2:c.125T>G	XP_005266460.1:p.Val42Gly
XM_005266404.2:c.125T>G	XP_005266461.1:p.Val42Gly
XM_006719827.2:c.125T>G	XP_006719890.1:p.Val42Gly
XM_011535096.1:c.125T>G	XP_011533398.1:p.Val42Gly
XM_005266401.3:c.125T>G	XP_005266458.1:p.Val42Gly
XM_005266403.3:c.125T>G	XP_005266460.1:p.Val42Gly
XM_005266404.3:c.125T>G	XP_005266461.1:p.Val42Gly
XM_006719827.3:c.125T>G	XP_006719890.1:p.Val42Gly
NM_001127217.3:c.125T>G MANE Select	NP_001120689.1:p.Val42Gly
NM_005905.6:c.125T>G	NP_005896.1:p.Val42Gly
NM_001378621.1:c.125T>G	NP_001365550.1:p.Val42Gly