Canonical Allele Identifier: CA338748109

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404487T>G (hg19) ; chr1:g.19077993T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19077993T>G , CM000663.2:g.19077993T>G	GRCh38
NC_000001.10:g.19404487T>G , CM000663.1:g.19404487T>G	GRCh37
NC_000001.9:g.19277074T>G	NCBI36
NG_027669.1:g.137260A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15307A>C MANE Select	ENSP00000364403.3:p.Ile5103Leu
ENST00000375224.1:c.2428A>C	ENSP00000364372.1:p.Ile810Leu
ENST00000375225.7:c.532A>C	ENSP00000364373.3:p.Ile178Leu
ENST00000375254.7:c.15307A>C	ENSP00000364403.3:p.Ile5103Leu
ENST00000459947.5:n.3314A>C
NM_020765.2:c.15307A>C	NP_065816.2:p.Ile5103Leu
XM_011541108.1:c.15460A>C	XP_011539410.1:p.Ile5154Leu
XM_011541109.1:c.15457A>C	XP_011539411.1:p.Ile5153Leu
XM_011541110.1:c.15457A>C	XP_011539412.1:p.Ile5153Leu
XM_011541111.1:c.15457A>C	XP_011539413.1:p.Ile5153Leu
XM_011541112.1:c.15445A>C	XP_011539414.1:p.Ile5149Leu
XM_011541113.1:c.15442A>C	XP_011539415.1:p.Ile5148Leu
XM_011541114.1:c.15442A>C	XP_011539416.1:p.Ile5148Leu
XM_011541115.1:c.15436A>C	XP_011539417.1:p.Ile5146Leu
XM_011541116.1:c.15427A>C	XP_011539418.1:p.Ile5143Leu
XM_011541117.1:c.15376A>C	XP_011539419.1:p.Ile5126Leu
XM_011541118.1:c.15373A>C	XP_011539420.1:p.Ile5125Leu
XM_011541119.1:c.15340A>C	XP_011539421.1:p.Ile5114Leu
XM_011541120.1:c.15337A>C	XP_011539422.1:p.Ile5113Leu
XM_011541121.1:c.15304A>C	XP_011539423.1:p.Ile5102Leu
XM_011541108.3:c.15574A>C	XP_011539410.2:p.Ile5192Leu
XM_011541109.3:c.15571A>C	XP_011539411.2:p.Ile5191Leu
XM_011541110.3:c.15571A>C	XP_011539412.2:p.Ile5191Leu
XM_011541111.3:c.15571A>C	XP_011539413.2:p.Ile5191Leu
XM_011541112.3:c.15559A>C	XP_011539414.2:p.Ile5187Leu
XM_011541113.3:c.15556A>C	XP_011539415.2:p.Ile5186Leu
XM_011541114.3:c.15556A>C	XP_011539416.2:p.Ile5186Leu
XM_011541115.3:c.15550A>C	XP_011539417.2:p.Ile5184Leu
XM_011541116.3:c.15541A>C	XP_011539418.2:p.Ile5181Leu
XM_011541117.3:c.15490A>C	XP_011539419.2:p.Ile5164Leu
XM_011541118.3:c.15487A>C	XP_011539420.2:p.Ile5163Leu
XM_011541119.3:c.15454A>C	XP_011539421.2:p.Ile5152Leu
XM_011541120.3:c.15451A>C	XP_011539422.2:p.Ile5151Leu
XM_011541121.3:c.15418A>C	XP_011539423.2:p.Ile5140Leu
XM_017000822.2:c.15553A>C	XP_016856311.2:p.Ile5185Leu
XM_017000823.2:c.15526A>C	XP_016856312.2:p.Ile5176Leu
XM_017000824.2:c.15472A>C	XP_016856313.2:p.Ile5158Leu
XM_017000825.2:c.15457A>C	XP_016856314.2:p.Ile5153Leu
XM_017000826.2:c.15454A>C	XP_016856315.2:p.Ile5152Leu
XM_017000827.2:c.15439A>C	XP_016856316.2:p.Ile5147Leu
XM_017000828.2:c.15415A>C	XP_016856317.2:p.Ile5139Leu
XM_017000829.2:c.15367A>C	XP_016856318.2:p.Ile5123Leu
XM_017000830.2:c.15316A>C	XP_016856319.2:p.Ile5106Leu
NM_020765.3:c.15307A>C MANE Select	NP_065816.2:p.Ile5103Leu