Canonical Allele Identifier: CA338748088

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404482G>T (hg19) ; chr1:g.19077988G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19077988G>T , CM000663.2:g.19077988G>T	GRCh38
NC_000001.10:g.19404482G>T , CM000663.1:g.19404482G>T	GRCh37
NC_000001.9:g.19277069G>T	NCBI36
NG_027669.1:g.137265C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15312C>A MANE Select	ENSP00000364403.3:p.Tyr5104Ter
ENST00000375224.1:c.2433C>A	ENSP00000364372.1:p.Tyr811Ter
ENST00000375225.7:c.537C>A	ENSP00000364373.3:p.Tyr179Ter
ENST00000375254.7:c.15312C>A	ENSP00000364403.3:p.Tyr5104Ter
ENST00000459947.5:n.3319C>A
NM_020765.2:c.15312C>A	NP_065816.2:p.Tyr5104Ter
XM_011541108.1:c.15465C>A	XP_011539410.1:p.Tyr5155Ter
XM_011541109.1:c.15462C>A	XP_011539411.1:p.Tyr5154Ter
XM_011541110.1:c.15462C>A	XP_011539412.1:p.Tyr5154Ter
XM_011541111.1:c.15462C>A	XP_011539413.1:p.Tyr5154Ter
XM_011541112.1:c.15450C>A	XP_011539414.1:p.Tyr5150Ter
XM_011541113.1:c.15447C>A	XP_011539415.1:p.Tyr5149Ter
XM_011541114.1:c.15447C>A	XP_011539416.1:p.Tyr5149Ter
XM_011541115.1:c.15441C>A	XP_011539417.1:p.Tyr5147Ter
XM_011541116.1:c.15432C>A	XP_011539418.1:p.Tyr5144Ter
XM_011541117.1:c.15381C>A	XP_011539419.1:p.Tyr5127Ter
XM_011541118.1:c.15378C>A	XP_011539420.1:p.Tyr5126Ter
XM_011541119.1:c.15345C>A	XP_011539421.1:p.Tyr5115Ter
XM_011541120.1:c.15342C>A	XP_011539422.1:p.Tyr5114Ter
XM_011541121.1:c.15309C>A	XP_011539423.1:p.Tyr5103Ter
XM_011541108.3:c.15579C>A	XP_011539410.2:p.Tyr5193Ter
XM_011541109.3:c.15576C>A	XP_011539411.2:p.Tyr5192Ter
XM_011541110.3:c.15576C>A	XP_011539412.2:p.Tyr5192Ter
XM_011541111.3:c.15576C>A	XP_011539413.2:p.Tyr5192Ter
XM_011541112.3:c.15564C>A	XP_011539414.2:p.Tyr5188Ter
XM_011541113.3:c.15561C>A	XP_011539415.2:p.Tyr5187Ter
XM_011541114.3:c.15561C>A	XP_011539416.2:p.Tyr5187Ter
XM_011541115.3:c.15555C>A	XP_011539417.2:p.Tyr5185Ter
XM_011541116.3:c.15546C>A	XP_011539418.2:p.Tyr5182Ter
XM_011541117.3:c.15495C>A	XP_011539419.2:p.Tyr5165Ter
XM_011541118.3:c.15492C>A	XP_011539420.2:p.Tyr5164Ter
XM_011541119.3:c.15459C>A	XP_011539421.2:p.Tyr5153Ter
XM_011541120.3:c.15456C>A	XP_011539422.2:p.Tyr5152Ter
XM_011541121.3:c.15423C>A	XP_011539423.2:p.Tyr5141Ter
XM_017000822.2:c.15558C>A	XP_016856311.2:p.Tyr5186Ter
XM_017000823.2:c.15531C>A	XP_016856312.2:p.Tyr5177Ter
XM_017000824.2:c.15477C>A	XP_016856313.2:p.Tyr5159Ter
XM_017000825.2:c.15462C>A	XP_016856314.2:p.Tyr5154Ter
XM_017000826.2:c.15459C>A	XP_016856315.2:p.Tyr5153Ter
XM_017000827.2:c.15444C>A	XP_016856316.2:p.Tyr5148Ter
XM_017000828.2:c.15420C>A	XP_016856317.2:p.Tyr5140Ter
XM_017000829.2:c.15372C>A	XP_016856318.2:p.Tyr5124Ter
XM_017000830.2:c.15321C>A	XP_016856319.2:p.Tyr5107Ter
NM_020765.3:c.15312C>A MANE Select	NP_065816.2:p.Tyr5104Ter