Canonical Allele Identifier: CA446540079
Gene: SMAD5 HGNC NCBI
SMAD5-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs3764941
MyVariant Identifiers: chr5:g.135469527T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.136133838T>A , CM000667.2:g.136133838T>A GRCh38
NC_000005.9:g.135469527T>A , CM000667.1:g.135469527T>A GRCh37
NC_000005.8:g.135497426T>A NCBI36
NG_032037.1:g.5992T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000509297.6:c.-366T>A (SMAD5) ENSP00000426696.2:n.-366T>A
ENST00000545279.6:c.-245+876T>A (SMAD5) MANE Select ENSP00000441954.2:n.-245+876T>A
ENST00000506223.1:c.-291T>A (SMAD5) ENSP00000422954.1:n.-291T>A
ENST00000507118.5:c.-170+876T>A (SMAD5) ENSP00000425749.1:n.-170+876T>A
ENST00000509297.5:c.-366T>A (SMAD5) ENSP00000426696.1:n.-366T>A
ENST00000509962.5:n.250+365T>A (SMAD5)
ENST00000511116.5:c.-329+876T>A (SMAD5) ENSP00000424279.1:n.-329+876T>A
ENST00000514777.1:n.59+876T>A (SMAD5)
ENST00000515005.1:c.-245+365T>A (SMAD5) ENSP00000427330.1:n.-245+365T>A
ENST00000545279.5:c.-245+876T>A (SMAD5) ENSP00000441954.2:n.-245+876T>A
ENST00000545620.5:c.-170+876T>A (SMAD5) ENSP00000446474.2:n.-170+876T>A
NM_001001419.2:c.-329+876T>A (SMAD5) NP_001001419.1:n.-329+876T>A
NM_001001420.2:c.-170+876T>A (SMAD5) NP_001001420.1:n.-170+876T>A
NM_005903.6:c.-245+876T>A (SMAD5) NP_005894.3:n.-245+876T>A
NR_026763.1:n.1053A>T (SMAD5-AS1)
XM_017009470.2:c.-329+365T>A (SMAD5) XP_016864959.1:n.-329+365T>A
XM_024446046.1:c.-245+365T>A (SMAD5) XP_024301814.1:n.-245+365T>A
XM_024446047.1:c.-366T>A (SMAD5) XP_024301815.1:n.-366T>A
NM_005903.7:c.-245+876T>A (SMAD5) MANE Select NP_005894.3:n.-245+876T>A
NM_001001419.3:c.-329+876T>A (SMAD5) NP_001001419.1:n.-329+876T>A
NM_001001420.3:c.-170+876T>A (SMAD5) NP_001001420.1:n.-170+876T>A