Canonical Allele Identifier: CA338748107

Gene: UBR4

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15307A>T MANE Select	ENSP00000364403.3:p.Ile5103Phe
ENST00000375224.1:c.2428A>T	ENSP00000364372.1:p.Ile810Phe
ENST00000375225.7:c.532A>T	ENSP00000364373.3:p.Ile178Phe
ENST00000375254.7:c.15307A>T	ENSP00000364403.3:p.Ile5103Phe
ENST00000459947.5:n.3314A>T
NM_020765.2:c.15307A>T	NP_065816.2:p.Ile5103Phe
XM_011541108.1:c.15460A>T	XP_011539410.1:p.Ile5154Phe
XM_011541109.1:c.15457A>T	XP_011539411.1:p.Ile5153Phe
XM_011541110.1:c.15457A>T	XP_011539412.1:p.Ile5153Phe
XM_011541111.1:c.15457A>T	XP_011539413.1:p.Ile5153Phe
XM_011541112.1:c.15445A>T	XP_011539414.1:p.Ile5149Phe
XM_011541113.1:c.15442A>T	XP_011539415.1:p.Ile5148Phe
XM_011541114.1:c.15442A>T	XP_011539416.1:p.Ile5148Phe
XM_011541115.1:c.15436A>T	XP_011539417.1:p.Ile5146Phe
XM_011541116.1:c.15427A>T	XP_011539418.1:p.Ile5143Phe
XM_011541117.1:c.15376A>T	XP_011539419.1:p.Ile5126Phe
XM_011541118.1:c.15373A>T	XP_011539420.1:p.Ile5125Phe
XM_011541119.1:c.15340A>T	XP_011539421.1:p.Ile5114Phe
XM_011541120.1:c.15337A>T	XP_011539422.1:p.Ile5113Phe
XM_011541121.1:c.15304A>T	XP_011539423.1:p.Ile5102Phe
XM_011541108.3:c.15574A>T	XP_011539410.2:p.Ile5192Phe
XM_011541109.3:c.15571A>T	XP_011539411.2:p.Ile5191Phe
XM_011541110.3:c.15571A>T	XP_011539412.2:p.Ile5191Phe
XM_011541111.3:c.15571A>T	XP_011539413.2:p.Ile5191Phe
XM_011541112.3:c.15559A>T	XP_011539414.2:p.Ile5187Phe
XM_011541113.3:c.15556A>T	XP_011539415.2:p.Ile5186Phe
XM_011541114.3:c.15556A>T	XP_011539416.2:p.Ile5186Phe
XM_011541115.3:c.15550A>T	XP_011539417.2:p.Ile5184Phe
XM_011541116.3:c.15541A>T	XP_011539418.2:p.Ile5181Phe
XM_011541117.3:c.15490A>T	XP_011539419.2:p.Ile5164Phe
XM_011541118.3:c.15487A>T	XP_011539420.2:p.Ile5163Phe
XM_011541119.3:c.15454A>T	XP_011539421.2:p.Ile5152Phe
XM_011541120.3:c.15451A>T	XP_011539422.2:p.Ile5151Phe
XM_011541121.3:c.15418A>T	XP_011539423.2:p.Ile5140Phe
XM_017000822.2:c.15553A>T	XP_016856311.2:p.Ile5185Phe
XM_017000823.2:c.15526A>T	XP_016856312.2:p.Ile5176Phe
XM_017000824.2:c.15472A>T	XP_016856313.2:p.Ile5158Phe
XM_017000825.2:c.15457A>T	XP_016856314.2:p.Ile5153Phe
XM_017000826.2:c.15454A>T	XP_016856315.2:p.Ile5152Phe
XM_017000827.2:c.15439A>T	XP_016856316.2:p.Ile5147Phe
XM_017000828.2:c.15415A>T	XP_016856317.2:p.Ile5139Phe
XM_017000829.2:c.15367A>T	XP_016856318.2:p.Ile5123Phe
XM_017000830.2:c.15316A>T	XP_016856319.2:p.Ile5106Phe
NM_020765.3:c.15307A>T MANE Select	NP_065816.2:p.Ile5103Phe