Canonical Allele Identifier: CA1156956076

Gene: UBR4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19078009C= , CM000663.2:g.19078009C=	GRCh38
NC_000001.10:g.19404503C= , CM000663.1:g.19404503C=	GRCh37
NC_000001.9:g.19277090C=	NCBI36
NG_027669.1:g.137244G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15291G= MANE Select	ENSP00000364403.3:p.Trp5097=
ENST00000375224.1:c.2412G=	ENSP00000364372.1:p.Trp804=
ENST00000375225.7:c.516G=	ENSP00000364373.3:p.Trp172=
ENST00000375254.7:c.15291G=	ENSP00000364403.3:p.Trp5097=
ENST00000459947.5:n.3298G=
NM_020765.2:c.15291G=	NP_065816.2:p.Trp5097=
XM_011541108.1:c.15444G=	XP_011539410.1:p.Trp5148=
XM_011541109.1:c.15441G=	XP_011539411.1:p.Trp5147=
XM_011541110.1:c.15441G=	XP_011539412.1:p.Trp5147=
XM_011541111.1:c.15441G=	XP_011539413.1:p.Trp5147=
XM_011541112.1:c.15429G=	XP_011539414.1:p.Trp5143=
XM_011541113.1:c.15426G=	XP_011539415.1:p.Trp5142=
XM_011541114.1:c.15426G=	XP_011539416.1:p.Trp5142=
XM_011541115.1:c.15420G=	XP_011539417.1:p.Trp5140=
XM_011541116.1:c.15411G=	XP_011539418.1:p.Trp5137=
XM_011541117.1:c.15360G=	XP_011539419.1:p.Trp5120=
XM_011541118.1:c.15357G=	XP_011539420.1:p.Trp5119=
XM_011541119.1:c.15324G=	XP_011539421.1:p.Trp5108=
XM_011541120.1:c.15321G=	XP_011539422.1:p.Trp5107=
XM_011541121.1:c.15288G=	XP_011539423.1:p.Trp5096=
XM_011541108.3:c.15558G=	XP_011539410.2:p.Trp5186=
XM_011541109.3:c.15555G=	XP_011539411.2:p.Trp5185=
XM_011541110.3:c.15555G=	XP_011539412.2:p.Trp5185=
XM_011541111.3:c.15555G=	XP_011539413.2:p.Trp5185=
XM_011541112.3:c.15543G=	XP_011539414.2:p.Trp5181=
XM_011541113.3:c.15540G=	XP_011539415.2:p.Trp5180=
XM_011541114.3:c.15540G=	XP_011539416.2:p.Trp5180=
XM_011541115.3:c.15534G=	XP_011539417.2:p.Trp5178=
XM_011541116.3:c.15525G=	XP_011539418.2:p.Trp5175=
XM_011541117.3:c.15474G=	XP_011539419.2:p.Trp5158=
XM_011541118.3:c.15471G=	XP_011539420.2:p.Trp5157=
XM_011541119.3:c.15438G=	XP_011539421.2:p.Trp5146=
XM_011541120.3:c.15435G=	XP_011539422.2:p.Trp5145=
XM_011541121.3:c.15402G=	XP_011539423.2:p.Trp5134=
XM_017000822.2:c.15537G=	XP_016856311.2:p.Trp5179=
XM_017000823.2:c.15510G=	XP_016856312.2:p.Trp5170=
XM_017000824.2:c.15456G=	XP_016856313.2:p.Trp5152=
XM_017000825.2:c.15441G=	XP_016856314.2:p.Trp5147=
XM_017000826.2:c.15438G=	XP_016856315.2:p.Trp5146=
XM_017000827.2:c.15423G=	XP_016856316.2:p.Trp5141=
XM_017000828.2:c.15399G=	XP_016856317.2:p.Trp5133=
XM_017000829.2:c.15351G=	XP_016856318.2:p.Trp5117=
XM_017000830.2:c.15300G=	XP_016856319.2:p.Trp5100=
NM_020765.3:c.15291G= MANE Select	NP_065816.2:p.Trp5097=