Canonical Allele Identifier: CA338748036

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404472T>A (hg19) ; chr1:g.19077978T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19077978T>A , CM000663.2:g.19077978T>A	GRCh38
NC_000001.10:g.19404472T>A , CM000663.1:g.19404472T>A	GRCh37
NC_000001.9:g.19277059T>A	NCBI36
NG_027669.1:g.137275A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15322A>T MANE Select	ENSP00000364403.3:p.Lys5108Ter
ENST00000375224.1:c.2443A>T	ENSP00000364372.1:p.Lys815Ter
ENST00000375225.7:c.547A>T	ENSP00000364373.3:p.Lys183Ter
ENST00000375254.7:c.15322A>T	ENSP00000364403.3:p.Lys5108Ter
ENST00000459947.5:n.3329A>T
NM_020765.2:c.15322A>T	NP_065816.2:p.Lys5108Ter
XM_011541108.1:c.15475A>T	XP_011539410.1:p.Lys5159Ter
XM_011541109.1:c.15472A>T	XP_011539411.1:p.Lys5158Ter
XM_011541110.1:c.15472A>T	XP_011539412.1:p.Lys5158Ter
XM_011541111.1:c.15472A>T	XP_011539413.1:p.Lys5158Ter
XM_011541112.1:c.15460A>T	XP_011539414.1:p.Lys5154Ter
XM_011541113.1:c.15457A>T	XP_011539415.1:p.Lys5153Ter
XM_011541114.1:c.15457A>T	XP_011539416.1:p.Lys5153Ter
XM_011541115.1:c.15451A>T	XP_011539417.1:p.Lys5151Ter
XM_011541116.1:c.15442A>T	XP_011539418.1:p.Lys5148Ter
XM_011541117.1:c.15391A>T	XP_011539419.1:p.Lys5131Ter
XM_011541118.1:c.15388A>T	XP_011539420.1:p.Lys5130Ter
XM_011541119.1:c.15355A>T	XP_011539421.1:p.Lys5119Ter
XM_011541120.1:c.15352A>T	XP_011539422.1:p.Lys5118Ter
XM_011541121.1:c.15319A>T	XP_011539423.1:p.Lys5107Ter
XM_011541108.3:c.15589A>T	XP_011539410.2:p.Lys5197Ter
XM_011541109.3:c.15586A>T	XP_011539411.2:p.Lys5196Ter
XM_011541110.3:c.15586A>T	XP_011539412.2:p.Lys5196Ter
XM_011541111.3:c.15586A>T	XP_011539413.2:p.Lys5196Ter
XM_011541112.3:c.15574A>T	XP_011539414.2:p.Lys5192Ter
XM_011541113.3:c.15571A>T	XP_011539415.2:p.Lys5191Ter
XM_011541114.3:c.15571A>T	XP_011539416.2:p.Lys5191Ter
XM_011541115.3:c.15565A>T	XP_011539417.2:p.Lys5189Ter
XM_011541116.3:c.15556A>T	XP_011539418.2:p.Lys5186Ter
XM_011541117.3:c.15505A>T	XP_011539419.2:p.Lys5169Ter
XM_011541118.3:c.15502A>T	XP_011539420.2:p.Lys5168Ter
XM_011541119.3:c.15469A>T	XP_011539421.2:p.Lys5157Ter
XM_011541120.3:c.15466A>T	XP_011539422.2:p.Lys5156Ter
XM_011541121.3:c.15433A>T	XP_011539423.2:p.Lys5145Ter
XM_017000822.2:c.15568A>T	XP_016856311.2:p.Lys5190Ter
XM_017000823.2:c.15541A>T	XP_016856312.2:p.Lys5181Ter
XM_017000824.2:c.15487A>T	XP_016856313.2:p.Lys5163Ter
XM_017000825.2:c.15472A>T	XP_016856314.2:p.Lys5158Ter
XM_017000826.2:c.15469A>T	XP_016856315.2:p.Lys5157Ter
XM_017000827.2:c.15454A>T	XP_016856316.2:p.Lys5152Ter
XM_017000828.2:c.15430A>T	XP_016856317.2:p.Lys5144Ter
XM_017000829.2:c.15382A>T	XP_016856318.2:p.Lys5128Ter
XM_017000830.2:c.15331A>T	XP_016856319.2:p.Lys5111Ter
NM_020765.3:c.15322A>T MANE Select	NP_065816.2:p.Lys5108Ter