Canonical Allele Identifier: CA2741438079

Gene: SMAD3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.67191334del , CM000677.2:g.67191334del	GRCh38
NC_000015.9:g.67483672del , CM000677.1:g.67483672del	GRCh37
NC_000015.8:g.65270726del	NCBI36
NG_011990.1:g.130478del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000558428.6:c.*798del	ENSP00000454165.2:n.*798del
ENST00000558739.2:c.*798del	ENSP00000453684.2:n.*798del
ENST00000558827.2:c.*798del	ENSP00000452767.2:n.*798del
ENST00000559460.6:c.*798del	ENSP00000453082.2:n.*798del
ENST00000560424.2:c.*798del	ENSP00000455540.2:n.*798del
ENST00000327367.9:c.*798del MANE Select	ENSP00000332973.4:n.*798del
ENST00000679624.1:c.*798del	ENSP00000505445.1:n.*798del
ENST00000681239.1:c.*798del	ENSP00000505641.1:n.*798del
ENST00000327367.8:c.*798del	ENSP00000332973.4:n.*798del
ENST00000558763.1:n.1770del
ENST00000560402.1:n.283-1539del
NM_001145102.1:c.*798del	NP_001138574.1:n.*798del
NM_001145103.1:c.*798del	NP_001138575.1:n.*798del
NM_001145104.1:c.*798del	NP_001138576.1:n.*798del
NM_005902.3:c.*798del	NP_005893.1:n.*798del
XM_011521559.1:c.*798del	XP_011519861.1:n.*798del
XM_011521560.1:c.*798del	XP_011519862.1:n.*798del
XM_011521559.3:c.*798del	XP_011519861.1:n.*798del
NM_005902.4:c.*798del MANE Select	NP_005893.1:n.*798del
NM_001145102.2:c.*798del	NP_001138574.1:n.*798del
NM_001145103.2:c.*798del	NP_001138575.1:n.*798del
NM_001145104.2:c.*798del	NP_001138576.1:n.*798del