Canonical Allele Identifier: CA416453017

Gene: UBR4

Linked Data

• COSMIC: COSM901406 ; COSM4867663 ; COSM4867664 ; COSM4867665
• MyVariant Identifiers: chr1:g.19404482G>A (hg19)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15312C>T MANE Select	ENSP00000364403.3:p.Tyr5104=
ENST00000375224.1:c.2433C>T	ENSP00000364372.1:p.Tyr811=
ENST00000375225.7:c.537C>T	ENSP00000364373.3:p.Tyr179=
ENST00000375254.7:c.15312C>T	ENSP00000364403.3:p.Tyr5104=
ENST00000459947.5:n.3319C>T
NM_020765.2:c.15312C>T	NP_065816.2:p.Tyr5104=
XM_011541108.1:c.15465C>T	XP_011539410.1:p.Tyr5155=
XM_011541109.1:c.15462C>T	XP_011539411.1:p.Tyr5154=
XM_011541110.1:c.15462C>T	XP_011539412.1:p.Tyr5154=
XM_011541111.1:c.15462C>T	XP_011539413.1:p.Tyr5154=
XM_011541112.1:c.15450C>T	XP_011539414.1:p.Tyr5150=
XM_011541113.1:c.15447C>T	XP_011539415.1:p.Tyr5149=
XM_011541114.1:c.15447C>T	XP_011539416.1:p.Tyr5149=
XM_011541115.1:c.15441C>T	XP_011539417.1:p.Tyr5147=
XM_011541116.1:c.15432C>T	XP_011539418.1:p.Tyr5144=
XM_011541117.1:c.15381C>T	XP_011539419.1:p.Tyr5127=
XM_011541118.1:c.15378C>T	XP_011539420.1:p.Tyr5126=
XM_011541119.1:c.15345C>T	XP_011539421.1:p.Tyr5115=
XM_011541120.1:c.15342C>T	XP_011539422.1:p.Tyr5114=
XM_011541121.1:c.15309C>T	XP_011539423.1:p.Tyr5103=
XM_011541108.3:c.15579C>T	XP_011539410.2:p.Tyr5193=
XM_011541109.3:c.15576C>T	XP_011539411.2:p.Tyr5192=
XM_011541110.3:c.15576C>T	XP_011539412.2:p.Tyr5192=
XM_011541111.3:c.15576C>T	XP_011539413.2:p.Tyr5192=
XM_011541112.3:c.15564C>T	XP_011539414.2:p.Tyr5188=
XM_011541113.3:c.15561C>T	XP_011539415.2:p.Tyr5187=
XM_011541114.3:c.15561C>T	XP_011539416.2:p.Tyr5187=
XM_011541115.3:c.15555C>T	XP_011539417.2:p.Tyr5185=
XM_011541116.3:c.15546C>T	XP_011539418.2:p.Tyr5182=
XM_011541117.3:c.15495C>T	XP_011539419.2:p.Tyr5165=
XM_011541118.3:c.15492C>T	XP_011539420.2:p.Tyr5164=
XM_011541119.3:c.15459C>T	XP_011539421.2:p.Tyr5153=
XM_011541120.3:c.15456C>T	XP_011539422.2:p.Tyr5152=
XM_011541121.3:c.15423C>T	XP_011539423.2:p.Tyr5141=
XM_017000822.2:c.15558C>T	XP_016856311.2:p.Tyr5186=
XM_017000823.2:c.15531C>T	XP_016856312.2:p.Tyr5177=
XM_017000824.2:c.15477C>T	XP_016856313.2:p.Tyr5159=
XM_017000825.2:c.15462C>T	XP_016856314.2:p.Tyr5154=
XM_017000826.2:c.15459C>T	XP_016856315.2:p.Tyr5153=
XM_017000827.2:c.15444C>T	XP_016856316.2:p.Tyr5148=
XM_017000828.2:c.15420C>T	XP_016856317.2:p.Tyr5140=
XM_017000829.2:c.15372C>T	XP_016856318.2:p.Tyr5124=
XM_017000830.2:c.15321C>T	XP_016856319.2:p.Tyr5107=
NM_020765.3:c.15312C>T MANE Select	NP_065816.2:p.Tyr5104=