Canonical Allele Identifier: CA2211942302

Gene: UMOD

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.20343100_20343101delinsAG , CM000678.2:g.20343100_20343101delinsAG	GRCh38
NC_000016.9:g.20354422_20354423delinsAG , CM000678.1:g.20354422_20354423delinsAG	GRCh37
NC_000016.8:g.20261923_20261924delinsAG	NCBI36
NG_008151.1:g.14615_14616delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396138.9:c.1331+923_1331+924delinsCT MANE Select	ENSP00000379442.5:n.1331+923_1331+924delinsCT
ENST00000302509.8:c.1331+923_1331+924delinsCT	ENSP00000306279.4:n.1331+923_1331+924delinsCT
ENST00000396134.6:c.1430+923_1430+924delinsCT	ENSP00000379438.2:n.1430+923_1430+924delinsCT
ENST00000396138.8:c.1478+923_1478+924delinsCT	ENSP00000379442.4:n.1478+923_1478+924delinsCT
ENST00000570689.5:c.1331+923_1331+924delinsCT	ENSP00000460548.1:n.1331+923_1331+924delinsCT
NM_001008389.2:c.1331+923_1331+924delinsCT	NP_001008390.1:n.1331+923_1331+924delinsCT
NM_001278614.1:c.1430+923_1430+924delinsCT	NP_001265543.1:n.1430+923_1430+924delinsCT
NM_003361.3:c.1331+923_1331+924delinsCT	NP_003352.2:n.1331+923_1331+924delinsCT
XM_011545934.1:c.1416-547_1416-546delinsCT	XP_011544236.1:n.1416-547_1416-546delinsCT
XM_011545935.1:c.1332-547_1332-546delinsCT	XP_011544237.1:n.1332-547_1332-546delinsCT
XM_011545936.1:c.1332-547_1332-546delinsCT	XP_011544238.1:n.1332-547_1332-546delinsCT
XM_011545937.1:c.1332-547_1332-546delinsCT	XP_011544239.1:n.1332-547_1332-546delinsCT
XM_011545938.1:c.1332-547_1332-546delinsCT	XP_011544240.1:n.1332-547_1332-546delinsCT
XM_011545939.1:c.1415+923_1415+924delinsCT	XP_011544241.1:n.1415+923_1415+924delinsCT
XM_011545940.1:c.1479-547_1479-546delinsCT	XP_011544242.1:n.1479-547_1479-546delinsCT
XM_011545934.2:c.1332-547_1332-546delinsCT	XP_011544236.2:n.1332-547_1332-546delinsCT
XM_011545940.2:c.1332-547_1332-546delinsCT	XP_011544242.2:n.1332-547_1332-546delinsCT
XM_024450433.1:c.1332-547_1332-546delinsCT	XP_024306201.1:n.1332-547_1332-546delinsCT
NM_001008389.3:c.1331+923_1331+924delinsCT	NP_001008390.1:n.1331+923_1331+924delinsCT
NM_001278614.2:c.1430+923_1430+924delinsCT	NP_001265543.1:n.1430+923_1430+924delinsCT
NM_001378232.1:c.1331+923_1331+924delinsCT	NP_001365161.1:n.1331+923_1331+924delinsCT
NM_001378233.1:c.1331+923_1331+924delinsCT	NP_001365162.1:n.1331+923_1331+924delinsCT
NM_001378234.1:c.1332-547_1332-546delinsCT	NP_001365163.1:n.1332-547_1332-546delinsCT
NM_001378235.1:c.1332-547_1332-546delinsCT	NP_001365164.1:n.1332-547_1332-546delinsCT
NM_003361.4:c.1331+923_1331+924delinsCT MANE Select	NP_003352.2:n.1331+923_1331+924delinsCT
NR_165456.1:n.1554+923_1554+924delinsCT