Canonical Allele Identifier: CA2211942229

Gene: UMOD

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.20343051A= , CM000678.2:g.20343051A=	GRCh38
NC_000016.9:g.20354373A= , CM000678.1:g.20354373A=	GRCh37
NC_000016.8:g.20261874A=	NCBI36
NG_008151.1:g.14665T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000396138.9:c.1331+973T= MANE Select	ENSP00000379442.5:n.1331+973T=
ENST00000302509.8:c.1331+973T=	ENSP00000306279.4:n.1331+973T=
ENST00000396134.6:c.1430+973T=	ENSP00000379438.2:n.1430+973T=
ENST00000396138.8:c.1478+973T=	ENSP00000379442.4:n.1478+973T=
ENST00000570689.5:c.1331+973T=	ENSP00000460548.1:n.1331+973T=
NM_001008389.2:c.1331+973T=	NP_001008390.1:n.1331+973T=
NM_001278614.1:c.1430+973T=	NP_001265543.1:n.1430+973T=
NM_003361.3:c.1331+973T=	NP_003352.2:n.1331+973T=
XM_011545934.1:c.1416-497T=	XP_011544236.1:n.1416-497T=
XM_011545935.1:c.1332-497T=	XP_011544237.1:n.1332-497T=
XM_011545936.1:c.1332-497T=	XP_011544238.1:n.1332-497T=
XM_011545937.1:c.1332-497T=	XP_011544239.1:n.1332-497T=
XM_011545938.1:c.1332-497T=	XP_011544240.1:n.1332-497T=
XM_011545939.1:c.1415+973T=	XP_011544241.1:n.1415+973T=
XM_011545940.1:c.1479-497T=	XP_011544242.1:n.1479-497T=
XM_011545934.2:c.1332-497T=	XP_011544236.2:n.1332-497T=
XM_011545940.2:c.1332-497T=	XP_011544242.2:n.1332-497T=
XM_024450433.1:c.1332-497T=	XP_024306201.1:n.1332-497T=
NM_001008389.3:c.1331+973T=	NP_001008390.1:n.1331+973T=
NM_001278614.2:c.1430+973T=	NP_001265543.1:n.1430+973T=
NM_001378232.1:c.1331+973T=	NP_001365161.1:n.1331+973T=
NM_001378233.1:c.1331+973T=	NP_001365162.1:n.1331+973T=
NM_001378234.1:c.1332-497T=	NP_001365163.1:n.1332-497T=
NM_001378235.1:c.1332-497T=	NP_001365164.1:n.1332-497T=
NM_003361.4:c.1331+973T= MANE Select	NP_003352.2:n.1331+973T=
NR_165456.1:n.1554+973T=