Canonical Allele Identifier: CA392956722

Gene: SMAD3

Linked Data

• MyVariant Identifiers: chr15:g.67477083A>T (hg19) ; chr15:g.67184745A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.67184745A>T , CM000677.2:g.67184745A>T	GRCh38
NC_000015.9:g.67477083A>T , CM000677.1:g.67477083A>T	GRCh37
NC_000015.8:g.65264137A>T	NCBI36
NG_011990.1:g.123889A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000558428.6:c.305A>T	ENSP00000454165.2:p.Tyr102Phe
ENST00000558739.2:c.575A>T	ENSP00000453684.2:p.Tyr192Phe
ENST00000558827.2:c.305A>T	ENSP00000452767.2:p.Tyr102Phe
ENST00000559460.6:c.575A>T	ENSP00000453082.2:p.Tyr192Phe
ENST00000560424.2:c.890A>T	ENSP00000455540.2:p.Tyr297Phe
ENST00000327367.9:c.890A>T MANE Select	ENSP00000332973.4:p.Tyr297Phe
ENST00000679624.1:c.575A>T	ENSP00000505445.1:p.Tyr192Phe
ENST00000680689.1:n.593A>T
ENST00000681239.1:c.575A>T	ENSP00000505641.1:p.Tyr192Phe
ENST00000327367.8:c.890A>T	ENSP00000332973.4:p.Tyr297Phe
ENST00000439724.7:c.758A>T	ENSP00000401133.3:p.Tyr253Phe
ENST00000537194.6:c.305A>T	ENSP00000445348.2:p.Tyr102Phe
ENST00000540846.6:c.575A>T	ENSP00000437757.2:p.Tyr192Phe
ENST00000558827.1:c.305A>T	ENSP00000452767.1:p.Tyr102Phe
ENST00000558894.5:c.557-2620A>T	ENSP00000458060.1:n.557-2620A>T
ENST00000560402.1:n.283-8128A>T
NM_001145102.1:c.575A>T	NP_001138574.1:p.Tyr192Phe
NM_001145103.1:c.758A>T	NP_001138575.1:p.Tyr253Phe
NM_001145104.1:c.305A>T	NP_001138576.1:p.Tyr102Phe
NM_005902.3:c.890A>T	NP_005893.1:p.Tyr297Phe
XM_011521559.1:c.758A>T	XP_011519861.1:p.Tyr253Phe
XM_011521560.1:c.743A>T	XP_011519862.1:p.Tyr248Phe
XM_011521559.3:c.758A>T	XP_011519861.1:p.Tyr253Phe
NM_005902.4:c.890A>T MANE Select	NP_005893.1:p.Tyr297Phe
NM_001145102.2:c.575A>T	NP_001138574.1:p.Tyr192Phe
NM_001145103.2:c.758A>T	NP_001138575.1:p.Tyr253Phe
NM_001145104.2:c.305A>T	NP_001138576.1:p.Tyr102Phe