Canonical Allele Identifier: CA416453028

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404485A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19077991A>G , CM000663.2:g.19077991A>G	GRCh38
NC_000001.10:g.19404485A>G , CM000663.1:g.19404485A>G	GRCh37
NC_000001.9:g.19277072A>G	NCBI36
NG_027669.1:g.137262T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15309T>C MANE Select	ENSP00000364403.3:p.Ile5103=
ENST00000375224.1:c.2430T>C	ENSP00000364372.1:p.Ile810=
ENST00000375225.7:c.534T>C	ENSP00000364373.3:p.Ile178=
ENST00000375254.7:c.15309T>C	ENSP00000364403.3:p.Ile5103=
ENST00000459947.5:n.3316T>C
NM_020765.2:c.15309T>C	NP_065816.2:p.Ile5103=
XM_011541108.1:c.15462T>C	XP_011539410.1:p.Ile5154=
XM_011541109.1:c.15459T>C	XP_011539411.1:p.Ile5153=
XM_011541110.1:c.15459T>C	XP_011539412.1:p.Ile5153=
XM_011541111.1:c.15459T>C	XP_011539413.1:p.Ile5153=
XM_011541112.1:c.15447T>C	XP_011539414.1:p.Ile5149=
XM_011541113.1:c.15444T>C	XP_011539415.1:p.Ile5148=
XM_011541114.1:c.15444T>C	XP_011539416.1:p.Ile5148=
XM_011541115.1:c.15438T>C	XP_011539417.1:p.Ile5146=
XM_011541116.1:c.15429T>C	XP_011539418.1:p.Ile5143=
XM_011541117.1:c.15378T>C	XP_011539419.1:p.Ile5126=
XM_011541118.1:c.15375T>C	XP_011539420.1:p.Ile5125=
XM_011541119.1:c.15342T>C	XP_011539421.1:p.Ile5114=
XM_011541120.1:c.15339T>C	XP_011539422.1:p.Ile5113=
XM_011541121.1:c.15306T>C	XP_011539423.1:p.Ile5102=
XM_011541108.3:c.15576T>C	XP_011539410.2:p.Ile5192=
XM_011541109.3:c.15573T>C	XP_011539411.2:p.Ile5191=
XM_011541110.3:c.15573T>C	XP_011539412.2:p.Ile5191=
XM_011541111.3:c.15573T>C	XP_011539413.2:p.Ile5191=
XM_011541112.3:c.15561T>C	XP_011539414.2:p.Ile5187=
XM_011541113.3:c.15558T>C	XP_011539415.2:p.Ile5186=
XM_011541114.3:c.15558T>C	XP_011539416.2:p.Ile5186=
XM_011541115.3:c.15552T>C	XP_011539417.2:p.Ile5184=
XM_011541116.3:c.15543T>C	XP_011539418.2:p.Ile5181=
XM_011541117.3:c.15492T>C	XP_011539419.2:p.Ile5164=
XM_011541118.3:c.15489T>C	XP_011539420.2:p.Ile5163=
XM_011541119.3:c.15456T>C	XP_011539421.2:p.Ile5152=
XM_011541120.3:c.15453T>C	XP_011539422.2:p.Ile5151=
XM_011541121.3:c.15420T>C	XP_011539423.2:p.Ile5140=
XM_017000822.2:c.15555T>C	XP_016856311.2:p.Ile5185=
XM_017000823.2:c.15528T>C	XP_016856312.2:p.Ile5176=
XM_017000824.2:c.15474T>C	XP_016856313.2:p.Ile5158=
XM_017000825.2:c.15459T>C	XP_016856314.2:p.Ile5153=
XM_017000826.2:c.15456T>C	XP_016856315.2:p.Ile5152=
XM_017000827.2:c.15441T>C	XP_016856316.2:p.Ile5147=
XM_017000828.2:c.15417T>C	XP_016856317.2:p.Ile5139=
XM_017000829.2:c.15369T>C	XP_016856318.2:p.Ile5123=
XM_017000830.2:c.15318T>C	XP_016856319.2:p.Ile5106=
NM_020765.3:c.15309T>C MANE Select	NP_065816.2:p.Ile5103=