Canonical Allele Identifier: CA1156956063

Gene: UBR4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19077983A= , CM000663.2:g.19077983A=	GRCh38
NC_000001.10:g.19404477A= , CM000663.1:g.19404477A=	GRCh37
NC_000001.9:g.19277064A=	NCBI36
NG_027669.1:g.137270T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15317T= MANE Select	ENSP00000364403.3:p.Met5106=
ENST00000375224.1:c.2438T=	ENSP00000364372.1:p.Met813=
ENST00000375225.7:c.542T=	ENSP00000364373.3:p.Met181=
ENST00000375254.7:c.15317T=	ENSP00000364403.3:p.Met5106=
ENST00000459947.5:n.3324T=
NM_020765.2:c.15317T=	NP_065816.2:p.Met5106=
XM_011541108.1:c.15470T=	XP_011539410.1:p.Met5157=
XM_011541109.1:c.15467T=	XP_011539411.1:p.Met5156=
XM_011541110.1:c.15467T=	XP_011539412.1:p.Met5156=
XM_011541111.1:c.15467T=	XP_011539413.1:p.Met5156=
XM_011541112.1:c.15455T=	XP_011539414.1:p.Met5152=
XM_011541113.1:c.15452T=	XP_011539415.1:p.Met5151=
XM_011541114.1:c.15452T=	XP_011539416.1:p.Met5151=
XM_011541115.1:c.15446T=	XP_011539417.1:p.Met5149=
XM_011541116.1:c.15437T=	XP_011539418.1:p.Met5146=
XM_011541117.1:c.15386T=	XP_011539419.1:p.Met5129=
XM_011541118.1:c.15383T=	XP_011539420.1:p.Met5128=
XM_011541119.1:c.15350T=	XP_011539421.1:p.Met5117=
XM_011541120.1:c.15347T=	XP_011539422.1:p.Met5116=
XM_011541121.1:c.15314T=	XP_011539423.1:p.Met5105=
XM_011541108.3:c.15584T=	XP_011539410.2:p.Met5195=
XM_011541109.3:c.15581T=	XP_011539411.2:p.Met5194=
XM_011541110.3:c.15581T=	XP_011539412.2:p.Met5194=
XM_011541111.3:c.15581T=	XP_011539413.2:p.Met5194=
XM_011541112.3:c.15569T=	XP_011539414.2:p.Met5190=
XM_011541113.3:c.15566T=	XP_011539415.2:p.Met5189=
XM_011541114.3:c.15566T=	XP_011539416.2:p.Met5189=
XM_011541115.3:c.15560T=	XP_011539417.2:p.Met5187=
XM_011541116.3:c.15551T=	XP_011539418.2:p.Met5184=
XM_011541117.3:c.15500T=	XP_011539419.2:p.Met5167=
XM_011541118.3:c.15497T=	XP_011539420.2:p.Met5166=
XM_011541119.3:c.15464T=	XP_011539421.2:p.Met5155=
XM_011541120.3:c.15461T=	XP_011539422.2:p.Met5154=
XM_011541121.3:c.15428T=	XP_011539423.2:p.Met5143=
XM_017000822.2:c.15563T=	XP_016856311.2:p.Met5188=
XM_017000823.2:c.15536T=	XP_016856312.2:p.Met5179=
XM_017000824.2:c.15482T=	XP_016856313.2:p.Met5161=
XM_017000825.2:c.15467T=	XP_016856314.2:p.Met5156=
XM_017000826.2:c.15464T=	XP_016856315.2:p.Met5155=
XM_017000827.2:c.15449T=	XP_016856316.2:p.Met5150=
XM_017000828.2:c.15425T=	XP_016856317.2:p.Met5142=
XM_017000829.2:c.15377T=	XP_016856318.2:p.Met5126=
XM_017000830.2:c.15326T=	XP_016856319.2:p.Met5109=
NM_020765.3:c.15317T= MANE Select	NP_065816.2:p.Met5106=