Canonical Allele Identifier: CA256248
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 12260
ClinVar RCV Id: RCV002251323
dbSNP Id: rs121917770

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.20348918T>C , CM000678.2:g.20348918T>C GRCh38
NC_000016.9:g.20360240T>C , CM000678.1:g.20360240T>C GRCh37
NC_000016.8:g.20267741T>C NCBI36
NG_008151.1:g.8798A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000396138.9:c.383A>G MANE Select ENSP00000379442.5:p.Asn128Ser
ENST00000302509.8:c.383A>G ENSP00000306279.4:p.Asn128Ser
ENST00000396134.6:c.482A>G ENSP00000379438.2:p.Asn161Ser
ENST00000396138.8:c.530A>G ENSP00000379442.4:p.Asn177Ser
ENST00000570689.5:c.383A>G ENSP00000460548.1:p.Asn128Ser
ENST00000573567.5:c.452A>G ENSP00000460374.1:p.Asn151Ser
NM_001008389.2:c.383A>G NP_001008390.1:p.Asn128Ser
NM_001278614.1:c.482A>G NP_001265543.1:p.Asn161Ser
NM_003361.3:c.383A>G NP_003352.2:p.Asn128Ser
XM_011545934.1:c.467A>G XP_011544236.1:p.Asn156Ser
XM_011545935.1:c.383A>G XP_011544237.1:p.Asn128Ser
XM_011545936.1:c.383A>G XP_011544238.1:p.Asn128Ser
XM_011545937.1:c.383A>G XP_011544239.1:p.Asn128Ser
XM_011545938.1:c.383A>G XP_011544240.1:p.Asn128Ser
XM_011545939.1:c.467A>G XP_011544241.1:p.Asn156Ser
XM_011545940.1:c.530A>G XP_011544242.1:p.Asn177Ser
XM_011545934.2:c.383A>G XP_011544236.2:p.Asn128Ser
XM_011545940.2:c.383A>G XP_011544242.2:p.Asn128Ser
XM_024450433.1:c.383A>G XP_024306201.1:p.Asn128Ser
NM_001008389.3:c.383A>G NP_001008390.1:p.Asn128Ser
NM_001278614.2:c.482A>G NP_001265543.1:p.Asn161Ser
NM_001378232.1:c.383A>G NP_001365161.1:p.Asn128Ser
NM_001378233.1:c.383A>G NP_001365162.1:p.Asn128Ser
NM_001378234.1:c.383A>G NP_001365163.1:p.Asn128Ser
NM_001378235.1:c.383A>G NP_001365164.1:p.Asn128Ser
NM_001378237.1:c.383A>G NP_001365166.1:p.Asn128Ser
NM_003361.4:c.383A>G MANE Select NP_003352.2:p.Asn128Ser
NR_165456.1:n.608A>G