Canonical Allele Identifier: CA7938981

Gene: UMOD

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.20333338G>A , CM000678.2:g.20333338G>A	GRCh38
NC_000016.9:g.20344660G>A , CM000678.1:g.20344660G>A	GRCh37
NC_000016.8:g.20252161G>A	NCBI36
NG_008151.1:g.24378C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_003361.4:c.1899C>T MANE Select	NP_003352.2:p.Ala633=
ENST00000396138.9:c.1899C>T MANE Select	ENSP00000379442.5:p.Ala633=
NM_001008389.2:c.1899C>T	NP_001008390.1:p.Ala633=
NM_001008389.3:c.1899C>T	NP_001008390.1:p.Ala633=
NM_001278614.1:c.1998C>T	NP_001265543.1:p.Ala666=
NM_001278614.2:c.1998C>T	NP_001265543.1:p.Ala666=
NM_001378232.1:c.1899C>T	NP_001365161.1:p.Ala633=
NM_001378233.1:c.1899C>T	NP_001365162.1:p.Ala633=
NM_001378234.1:c.2040C>T	NP_001365163.1:p.Ala680=
NM_001378235.1:c.2040C>T	NP_001365164.1:p.Ala680=
NM_003361.3:c.1899C>T	NP_003352.2:p.Ala633=
NR_165456.1:n.2122C>T
ENST00000302509.8:c.1899C>T	ENSP00000306279.4:p.Ala633=
ENST00000396134.6:c.1998C>T	ENSP00000379438.2:p.Ala666=
ENST00000396138.8:c.2046C>T	ENSP00000379442.4:p.Ala682=
ENST00000570689.5:c.1899C>T	ENSP00000460548.1:p.Ala633=
XM_011545934.1:c.2124C>T	XP_011544236.1:p.Ala708=
XM_011545934.2:c.2040C>T	XP_011544236.2:p.Ala680=
XM_011545935.1:c.2040C>T	XP_011544237.1:p.Ala680=
XM_011545936.1:c.2040C>T	XP_011544238.1:p.Ala680=
XM_011545937.1:c.2040C>T	XP_011544239.1:p.Ala680=
XM_011545938.1:c.2040C>T	XP_011544240.1:p.Ala680=
XM_011545939.1:c.1983C>T	XP_011544241.1:p.Ala661=
XM_011545940.1:c.2187C>T	XP_011544242.1:p.Ala729=
XM_011545940.2:c.2040C>T	XP_011544242.2:p.Ala680=
XM_024450433.1:c.2040C>T	XP_024306201.1:p.Ala680=