Canonical Allele Identifier: CA7939034

Gene: UMOD

Linked Data

• ClinVar Variation Id: 318284
• ClinVar RCV Id: RCV002520990 ; RCV002251351 ; RCV004021646
• dbSNP Id: rs143641292
• ExAC: 16:20348048 G / T
• gnomAD v2: 16-20348048-G-T
• gnomAD v3: 16-20336726-G-T
• gnomAD v4: 16-20336726-G-T
• MyVariant Identifiers: chr16:g.20348048G>T (hg19) ; chr16:g.20336726G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.20336726G>T , CM000678.2:g.20336726G>T	GRCh38
NC_000016.9:g.20348048G>T , CM000678.1:g.20348048G>T	GRCh37
NC_000016.8:g.20255549G>T	NCBI36
NG_008151.1:g.20990C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396138.9:c.1742C>A MANE Select	ENSP00000379442.5:p.Thr581Asn
ENST00000302509.8:c.1742C>A	ENSP00000306279.4:p.Thr581Asn
ENST00000396134.6:c.1841C>A	ENSP00000379438.2:p.Thr614Asn
ENST00000396138.8:c.1889C>A	ENSP00000379442.4:p.Thr630Asn
ENST00000570331.1:n.507C>A
ENST00000570689.5:c.1742C>A	ENSP00000460548.1:p.Thr581Asn
NM_001008389.2:c.1742C>A	NP_001008390.1:p.Thr581Asn
NM_001278614.1:c.1841C>A	NP_001265543.1:p.Thr614Asn
NM_003361.3:c.1742C>A	NP_003352.2:p.Thr581Asn
XM_011545934.1:c.1967C>A	XP_011544236.1:p.Thr656Asn
XM_011545935.1:c.1883C>A	XP_011544237.1:p.Thr628Asn
XM_011545936.1:c.1883C>A	XP_011544238.1:p.Thr628Asn
XM_011545937.1:c.1883C>A	XP_011544239.1:p.Thr628Asn
XM_011545938.1:c.1883C>A	XP_011544240.1:p.Thr628Asn
XM_011545939.1:c.1826C>A	XP_011544241.1:p.Thr609Asn
XM_011545940.1:c.2030C>A	XP_011544242.1:p.Thr677Asn
XM_011545934.2:c.1883C>A	XP_011544236.2:p.Thr628Asn
XM_011545940.2:c.1883C>A	XP_011544242.2:p.Thr628Asn
XM_024450433.1:c.1883C>A	XP_024306201.1:p.Thr628Asn
NM_001008389.3:c.1742C>A	NP_001008390.1:p.Thr581Asn
NM_001278614.2:c.1841C>A	NP_001265543.1:p.Thr614Asn
NM_001378232.1:c.1742C>A	NP_001365161.1:p.Thr581Asn
NM_001378233.1:c.1742C>A	NP_001365162.1:p.Thr581Asn
NM_001378234.1:c.1883C>A	NP_001365163.1:p.Thr628Asn
NM_001378235.1:c.1883C>A	NP_001365164.1:p.Thr628Asn
NM_003361.4:c.1742C>A MANE Select	NP_003352.2:p.Thr581Asn
NR_165456.1:n.1965C>A