Canonical Allele Identifier: CA1584823481

Gene: SMAD5 SMAD5-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.136134658_136134660delinsCTT , CM000667.2:g.136134658_136134660delinsCTT	GRCh38
NC_000005.9:g.135470347_135470349delinsCTT , CM000667.1:g.135470347_135470349delinsCTT	GRCh37
NC_000005.8:g.135498246_135498248delinsCTT	NCBI36
NG_032037.1:g.6812_6814delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509297.6:c.-245+699_-245+701delinsCTT (SMAD5)	ENSP00000426696.2:n.-245+699_-245+701delinsCTT
ENST00000545279.6:c.-245+1696_-245+1698delinsCTT (SMAD5) MANE Select	ENSP00000441954.2:n.-245+1696_-245+1698delinsCTT
ENST00000506223.1:c.-170+699_-170+701delinsCTT (SMAD5)	ENSP00000422954.1:n.-170+699_-170+701delinsCTT
ENST00000507118.5:c.-170+1696_-170+1698delinsCTT (SMAD5)	ENSP00000425749.1:n.-170+1696_-170+1698delinsCTT
ENST00000509297.5:c.-245+699_-245+701delinsCTT (SMAD5)	ENSP00000426696.1:n.-245+699_-245+701delinsCTT
ENST00000509962.5:n.250+1185_250+1187delinsCTT (SMAD5)
ENST00000511116.5:c.-329+1696_-329+1698delinsCTT (SMAD5)	ENSP00000424279.1:n.-329+1696_-329+1698delinsCTT
ENST00000514777.1:n.59+1696_59+1698delinsCTT (SMAD5)
ENST00000515005.1:c.-245+1185_-245+1187delinsCTT (SMAD5)	ENSP00000427330.1:n.-245+1185_-245+1187delinsCTT
ENST00000545279.5:c.-245+1696_-245+1698delinsCTT (SMAD5)	ENSP00000441954.2:n.-245+1696_-245+1698delinsCTT
ENST00000545620.5:c.-170+1696_-170+1698delinsCTT (SMAD5)	ENSP00000446474.2:n.-170+1696_-170+1698delinsCTT
NM_001001419.2:c.-329+1696_-329+1698delinsCTT (SMAD5)	NP_001001419.1:n.-329+1696_-329+1698delinsCTT
NM_001001420.2:c.-170+1696_-170+1698delinsCTT (SMAD5)	NP_001001420.1:n.-170+1696_-170+1698delinsCTT
NM_005903.6:c.-245+1696_-245+1698delinsCTT (SMAD5)	NP_005894.3:n.-245+1696_-245+1698delinsCTT
NR_026763.1:n.231_233delinsAAG (SMAD5-AS1)
XM_017009470.2:c.-329+1185_-329+1187delinsCTT (SMAD5)	XP_016864959.1:n.-329+1185_-329+1187delinsCTT
XM_024446046.1:c.-245+1185_-245+1187delinsCTT (SMAD5)	XP_024301814.1:n.-245+1185_-245+1187delinsCTT
XM_024446047.1:c.-245+699_-245+701delinsCTT (SMAD5)	XP_024301815.1:n.-245+699_-245+701delinsCTT
NM_005903.7:c.-245+1696_-245+1698delinsCTT (SMAD5) MANE Select	NP_005894.3:n.-245+1696_-245+1698delinsCTT
NM_001001419.3:c.-329+1696_-329+1698delinsCTT (SMAD5)	NP_001001419.1:n.-329+1696_-329+1698delinsCTT
NM_001001420.3:c.-170+1696_-170+1698delinsCTT (SMAD5)	NP_001001420.1:n.-170+1696_-170+1698delinsCTT