Canonical Allele Identifier: CA338748104

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404486A>G (hg19) ; chr1:g.19077992A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19077992A>G , CM000663.2:g.19077992A>G	GRCh38
NC_000001.10:g.19404486A>G , CM000663.1:g.19404486A>G	GRCh37
NC_000001.9:g.19277073A>G	NCBI36
NG_027669.1:g.137261T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15308T>C MANE Select	ENSP00000364403.3:p.Ile5103Thr
ENST00000375224.1:c.2429T>C	ENSP00000364372.1:p.Ile810Thr
ENST00000375225.7:c.533T>C	ENSP00000364373.3:p.Ile178Thr
ENST00000375254.7:c.15308T>C	ENSP00000364403.3:p.Ile5103Thr
ENST00000459947.5:n.3315T>C
NM_020765.2:c.15308T>C	NP_065816.2:p.Ile5103Thr
XM_011541108.1:c.15461T>C	XP_011539410.1:p.Ile5154Thr
XM_011541109.1:c.15458T>C	XP_011539411.1:p.Ile5153Thr
XM_011541110.1:c.15458T>C	XP_011539412.1:p.Ile5153Thr
XM_011541111.1:c.15458T>C	XP_011539413.1:p.Ile5153Thr
XM_011541112.1:c.15446T>C	XP_011539414.1:p.Ile5149Thr
XM_011541113.1:c.15443T>C	XP_011539415.1:p.Ile5148Thr
XM_011541114.1:c.15443T>C	XP_011539416.1:p.Ile5148Thr
XM_011541115.1:c.15437T>C	XP_011539417.1:p.Ile5146Thr
XM_011541116.1:c.15428T>C	XP_011539418.1:p.Ile5143Thr
XM_011541117.1:c.15377T>C	XP_011539419.1:p.Ile5126Thr
XM_011541118.1:c.15374T>C	XP_011539420.1:p.Ile5125Thr
XM_011541119.1:c.15341T>C	XP_011539421.1:p.Ile5114Thr
XM_011541120.1:c.15338T>C	XP_011539422.1:p.Ile5113Thr
XM_011541121.1:c.15305T>C	XP_011539423.1:p.Ile5102Thr
XM_011541108.3:c.15575T>C	XP_011539410.2:p.Ile5192Thr
XM_011541109.3:c.15572T>C	XP_011539411.2:p.Ile5191Thr
XM_011541110.3:c.15572T>C	XP_011539412.2:p.Ile5191Thr
XM_011541111.3:c.15572T>C	XP_011539413.2:p.Ile5191Thr
XM_011541112.3:c.15560T>C	XP_011539414.2:p.Ile5187Thr
XM_011541113.3:c.15557T>C	XP_011539415.2:p.Ile5186Thr
XM_011541114.3:c.15557T>C	XP_011539416.2:p.Ile5186Thr
XM_011541115.3:c.15551T>C	XP_011539417.2:p.Ile5184Thr
XM_011541116.3:c.15542T>C	XP_011539418.2:p.Ile5181Thr
XM_011541117.3:c.15491T>C	XP_011539419.2:p.Ile5164Thr
XM_011541118.3:c.15488T>C	XP_011539420.2:p.Ile5163Thr
XM_011541119.3:c.15455T>C	XP_011539421.2:p.Ile5152Thr
XM_011541120.3:c.15452T>C	XP_011539422.2:p.Ile5151Thr
XM_011541121.3:c.15419T>C	XP_011539423.2:p.Ile5140Thr
XM_017000822.2:c.15554T>C	XP_016856311.2:p.Ile5185Thr
XM_017000823.2:c.15527T>C	XP_016856312.2:p.Ile5176Thr
XM_017000824.2:c.15473T>C	XP_016856313.2:p.Ile5158Thr
XM_017000825.2:c.15458T>C	XP_016856314.2:p.Ile5153Thr
XM_017000826.2:c.15455T>C	XP_016856315.2:p.Ile5152Thr
XM_017000827.2:c.15440T>C	XP_016856316.2:p.Ile5147Thr
XM_017000828.2:c.15416T>C	XP_016856317.2:p.Ile5139Thr
XM_017000829.2:c.15368T>C	XP_016856318.2:p.Ile5123Thr
XM_017000830.2:c.15317T>C	XP_016856319.2:p.Ile5106Thr
NM_020765.3:c.15308T>C MANE Select	NP_065816.2:p.Ile5103Thr