Canonical Allele Identifier: CA2184377939

Gene: SMAD3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.67093131C= , CM000677.2:g.67093131C=	GRCh38
NC_000015.9:g.67385469C= , CM000677.1:g.67385469C=	GRCh37
NC_000015.8:g.65172523C=	NCBI36
NG_011990.1:g.32275C=

Transcript Alleles

HGVS	Amino-acid Change
NM_005902.4:c.206+26771C= MANE Select	NP_005893.1:n.206+26771C=
ENST00000327367.9:c.206+26771C= MANE Select	ENSP00000332973.4:n.206+26771C=
NM_005902.3:c.206+26771C=	NP_005893.1:n.206+26771C=
ENST00000327367.8:c.206+26771C=	ENSP00000332973.4:n.206+26771C=
ENST00000559460.5:c.-110+29187C=	ENSP00000453082.1:n.-110+29187C=
ENST00000559460.6:c.-110+29187C=	ENSP00000453082.2:n.-110+29187C=
ENST00000559937.1:n.56+15090C=
ENST00000560424.2:c.206+26771C=	ENSP00000455540.2:n.206+26771C=
ENST00000679624.1:c.-110+25218C=	ENSP00000505445.1:n.-110+25218C=
XM_011521559.1:c.206+26771C=	XP_011519861.1:n.206+26771C=
XM_011521559.3:c.206+26771C=	XP_011519861.1:n.206+26771C=