Canonical Allele Identifier: CA279294315
Gene: UMOD HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs183962941

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.20343125G>A , CM000678.2:g.20343125G>A GRCh38
NC_000016.8:g.20261948G>A NCBI36
NC_000016.9:g.20354447G>A , CM000678.1:g.20354447G>A GRCh37
NG_008151.1:g.14591C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000302509.8:c.1331+899C>T ENSP00000306279.4:p.=
ENST00000396134.6:c.1430+899C>T ENSP00000379438.2:p.=
ENST00000396138.8:c.1478+899C>T ENSP00000379442.4:p.=
ENST00000570689.5:c.1331+899C>T ENSP00000460548.1:p.=
NM_001008389.2:c.1331+899C>T VV NP_001008390.1:p.=
NM_001278614.1:c.1430+899C>T VV NP_001265543.1:p.=
NM_003361.3:c.1331+899C>T VV NP_003352.2:p.=
XM_011545934.1:c.1416-571C>T XP_011544236.1:p.=
XM_011545935.1:c.1332-571C>T XP_011544237.1:p.=
XM_011545936.1:c.1332-571C>T XP_011544238.1:p.=
XM_011545937.1:c.1332-571C>T XP_011544239.1:p.=
XM_011545938.1:c.1332-571C>T XP_011544240.1:p.=
XM_011545939.1:c.1415+899C>T XP_011544241.1:p.=
XM_011545940.1:c.1479-571C>T XP_011544242.1:p.=