Canonical Allele Identifier: CA416453160

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404533A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19078039A>G , CM000663.2:g.19078039A>G	GRCh38
NC_000001.10:g.19404533A>G , CM000663.1:g.19404533A>G	GRCh37
NC_000001.9:g.19277120A>G	NCBI36
NG_027669.1:g.137214T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15261T>C MANE Select	ENSP00000364403.3:p.Tyr5087=
ENST00000375224.1:c.2382T>C	ENSP00000364372.1:p.Tyr794=
ENST00000375225.7:c.486T>C	ENSP00000364373.3:p.Tyr162=
ENST00000375254.7:c.15261T>C	ENSP00000364403.3:p.Tyr5087=
ENST00000459947.5:n.3268T>C
NM_020765.2:c.15261T>C	NP_065816.2:p.Tyr5087=
XM_011541108.1:c.15414T>C	XP_011539410.1:p.Tyr5138=
XM_011541109.1:c.15411T>C	XP_011539411.1:p.Tyr5137=
XM_011541110.1:c.15411T>C	XP_011539412.1:p.Tyr5137=
XM_011541111.1:c.15411T>C	XP_011539413.1:p.Tyr5137=
XM_011541112.1:c.15399T>C	XP_011539414.1:p.Tyr5133=
XM_011541113.1:c.15396T>C	XP_011539415.1:p.Tyr5132=
XM_011541114.1:c.15396T>C	XP_011539416.1:p.Tyr5132=
XM_011541115.1:c.15390T>C	XP_011539417.1:p.Tyr5130=
XM_011541116.1:c.15381T>C	XP_011539418.1:p.Tyr5127=
XM_011541117.1:c.15330T>C	XP_011539419.1:p.Tyr5110=
XM_011541118.1:c.15327T>C	XP_011539420.1:p.Tyr5109=
XM_011541119.1:c.15294T>C	XP_011539421.1:p.Tyr5098=
XM_011541120.1:c.15291T>C	XP_011539422.1:p.Tyr5097=
XM_011541121.1:c.15258T>C	XP_011539423.1:p.Tyr5086=
XM_011541108.3:c.15528T>C	XP_011539410.2:p.Tyr5176=
XM_011541109.3:c.15525T>C	XP_011539411.2:p.Tyr5175=
XM_011541110.3:c.15525T>C	XP_011539412.2:p.Tyr5175=
XM_011541111.3:c.15525T>C	XP_011539413.2:p.Tyr5175=
XM_011541112.3:c.15513T>C	XP_011539414.2:p.Tyr5171=
XM_011541113.3:c.15510T>C	XP_011539415.2:p.Tyr5170=
XM_011541114.3:c.15510T>C	XP_011539416.2:p.Tyr5170=
XM_011541115.3:c.15504T>C	XP_011539417.2:p.Tyr5168=
XM_011541116.3:c.15495T>C	XP_011539418.2:p.Tyr5165=
XM_011541117.3:c.15444T>C	XP_011539419.2:p.Tyr5148=
XM_011541118.3:c.15441T>C	XP_011539420.2:p.Tyr5147=
XM_011541119.3:c.15408T>C	XP_011539421.2:p.Tyr5136=
XM_011541120.3:c.15405T>C	XP_011539422.2:p.Tyr5135=
XM_011541121.3:c.15372T>C	XP_011539423.2:p.Tyr5124=
XM_017000822.2:c.15507T>C	XP_016856311.2:p.Tyr5169=
XM_017000823.2:c.15480T>C	XP_016856312.2:p.Tyr5160=
XM_017000824.2:c.15426T>C	XP_016856313.2:p.Tyr5142=
XM_017000825.2:c.15411T>C	XP_016856314.2:p.Tyr5137=
XM_017000826.2:c.15408T>C	XP_016856315.2:p.Tyr5136=
XM_017000827.2:c.15393T>C	XP_016856316.2:p.Tyr5131=
XM_017000828.2:c.15369T>C	XP_016856317.2:p.Tyr5123=
XM_017000829.2:c.15321T>C	XP_016856318.2:p.Tyr5107=
XM_017000830.2:c.15270T>C	XP_016856319.2:p.Tyr5090=
NM_020765.3:c.15261T>C MANE Select	NP_065816.2:p.Tyr5087=