Canonical Allele Identifier: CA1584823766
Gene: SMAD5 HGNC NCBI
SMAD5-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.136134868G= , CM000667.2:g.136134868G= GRCh38
NC_000005.9:g.135470557G= , CM000667.1:g.135470557G= GRCh37
NC_000005.8:g.135498456G= NCBI36
NG_032037.1:g.7022G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000509297.6:c.-245+909G= (SMAD5) ENSP00000426696.2:n.-245+909G=
ENST00000545279.6:c.-245+1906G= (SMAD5) MANE Select ENSP00000441954.2:n.-245+1906G=
ENST00000506223.1:c.-170+909G= (SMAD5) ENSP00000422954.1:n.-170+909G=
ENST00000507118.5:c.-170+1906G= (SMAD5) ENSP00000425749.1:n.-170+1906G=
ENST00000509297.5:c.-245+909G= (SMAD5) ENSP00000426696.1:n.-245+909G=
ENST00000509962.5:n.250+1395G= (SMAD5)
ENST00000511116.5:c.-329+1906G= (SMAD5) ENSP00000424279.1:n.-329+1906G=
ENST00000514777.1:n.59+1906G= (SMAD5)
ENST00000515005.1:c.-245+1395G= (SMAD5) ENSP00000427330.1:n.-245+1395G=
ENST00000545279.5:c.-245+1906G= (SMAD5) ENSP00000441954.2:n.-245+1906G=
ENST00000545620.5:c.-170+1906G= (SMAD5) ENSP00000446474.2:n.-170+1906G=
NM_001001419.2:c.-329+1906G= (SMAD5) NP_001001419.1:n.-329+1906G=
NM_001001420.2:c.-170+1906G= (SMAD5) NP_001001420.1:n.-170+1906G=
NM_005903.6:c.-245+1906G= (SMAD5) NP_005894.3:n.-245+1906G=
NR_026763.1:n.23C= (SMAD5-AS1)
XM_017009470.2:c.-329+1395G= (SMAD5) XP_016864959.1:n.-329+1395G=
XM_024446046.1:c.-245+1395G= (SMAD5) XP_024301814.1:n.-245+1395G=
XM_024446047.1:c.-245+909G= (SMAD5) XP_024301815.1:n.-245+909G=
NM_005903.7:c.-245+1906G= (SMAD5) MANE Select NP_005894.3:n.-245+1906G=
NM_001001419.3:c.-329+1906G= (SMAD5) NP_001001419.1:n.-329+1906G=
NM_001001420.3:c.-170+1906G= (SMAD5) NP_001001420.1:n.-170+1906G=