Canonical Allele Identifier: CA16609689

Gene: SMAD7

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.48927093T= , CM000680.2:g.48927093T=	GRCh38
NC_000018.9:g.46453463T= , CM000680.1:g.46453463T=	GRCh37
NC_000018.8:g.44707461T=	NCBI36
NG_023330.1:g.28619A=

Transcript Alleles

HGVS	Amino-acid Change
NM_005904.4:c.743-5183A= MANE Select	NP_005895.1:n.743-5183A=
ENST00000262158.8:c.743-5183A= MANE Select	ENSP00000262158.2:n.743-5183A=
NM_001190821.1:c.740-5183A=	NP_001177750.1:n.740-5183A=
NM_001190821.2:c.740-5183A=	NP_001177750.1:n.740-5183A=
NM_001190822.1:c.98-5183A=	NP_001177751.1:n.98-5183A=
NM_001190822.2:c.98-5183A=	NP_001177751.1:n.98-5183A=
NM_001190823.1:c.179-5183A=	NP_001177752.1:n.179-5183A=
NM_001190823.2:c.179-5183A=	NP_001177752.1:n.179-5183A=
NM_005904.3:c.743-5183A=	NP_005895.1:n.743-5183A=
ENST00000262158.6:c.743-5183A=	ENSP00000262158.2:n.743-5183A=
ENST00000262158.7:c.743-5183A=	ENSP00000262158.2:n.743-5183A=
ENST00000545051.2:n.328-5183A=
ENST00000585986.1:n.154-5183A=
ENST00000586093.1:c.98-5183A=	ENSP00000465590.1:n.98-5183A=
ENST00000587336.1:n.49+3041A=
ENST00000588190.1:n.132-5183A=
ENST00000589634.1:c.740-5183A=	ENSP00000467621.1:n.740-5183A=
ENST00000591805.5:c.98-5183A=	ENSP00000466902.1:n.98-5183A=