Canonical Allele Identifier: CA338748151

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404503C>G (hg19) ; chr1:g.19078009C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19078009C>G , CM000663.2:g.19078009C>G	GRCh38
NC_000001.10:g.19404503C>G , CM000663.1:g.19404503C>G	GRCh37
NC_000001.9:g.19277090C>G	NCBI36
NG_027669.1:g.137244G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15291G>C MANE Select	ENSP00000364403.3:p.Trp5097Cys
ENST00000375224.1:c.2412G>C	ENSP00000364372.1:p.Trp804Cys
ENST00000375225.7:c.516G>C	ENSP00000364373.3:p.Trp172Cys
ENST00000375254.7:c.15291G>C	ENSP00000364403.3:p.Trp5097Cys
ENST00000459947.5:n.3298G>C
NM_020765.2:c.15291G>C	NP_065816.2:p.Trp5097Cys
XM_011541108.1:c.15444G>C	XP_011539410.1:p.Trp5148Cys
XM_011541109.1:c.15441G>C	XP_011539411.1:p.Trp5147Cys
XM_011541110.1:c.15441G>C	XP_011539412.1:p.Trp5147Cys
XM_011541111.1:c.15441G>C	XP_011539413.1:p.Trp5147Cys
XM_011541112.1:c.15429G>C	XP_011539414.1:p.Trp5143Cys
XM_011541113.1:c.15426G>C	XP_011539415.1:p.Trp5142Cys
XM_011541114.1:c.15426G>C	XP_011539416.1:p.Trp5142Cys
XM_011541115.1:c.15420G>C	XP_011539417.1:p.Trp5140Cys
XM_011541116.1:c.15411G>C	XP_011539418.1:p.Trp5137Cys
XM_011541117.1:c.15360G>C	XP_011539419.1:p.Trp5120Cys
XM_011541118.1:c.15357G>C	XP_011539420.1:p.Trp5119Cys
XM_011541119.1:c.15324G>C	XP_011539421.1:p.Trp5108Cys
XM_011541120.1:c.15321G>C	XP_011539422.1:p.Trp5107Cys
XM_011541121.1:c.15288G>C	XP_011539423.1:p.Trp5096Cys
XM_011541108.3:c.15558G>C	XP_011539410.2:p.Trp5186Cys
XM_011541109.3:c.15555G>C	XP_011539411.2:p.Trp5185Cys
XM_011541110.3:c.15555G>C	XP_011539412.2:p.Trp5185Cys
XM_011541111.3:c.15555G>C	XP_011539413.2:p.Trp5185Cys
XM_011541112.3:c.15543G>C	XP_011539414.2:p.Trp5181Cys
XM_011541113.3:c.15540G>C	XP_011539415.2:p.Trp5180Cys
XM_011541114.3:c.15540G>C	XP_011539416.2:p.Trp5180Cys
XM_011541115.3:c.15534G>C	XP_011539417.2:p.Trp5178Cys
XM_011541116.3:c.15525G>C	XP_011539418.2:p.Trp5175Cys
XM_011541117.3:c.15474G>C	XP_011539419.2:p.Trp5158Cys
XM_011541118.3:c.15471G>C	XP_011539420.2:p.Trp5157Cys
XM_011541119.3:c.15438G>C	XP_011539421.2:p.Trp5146Cys
XM_011541120.3:c.15435G>C	XP_011539422.2:p.Trp5145Cys
XM_011541121.3:c.15402G>C	XP_011539423.2:p.Trp5134Cys
XM_017000822.2:c.15537G>C	XP_016856311.2:p.Trp5179Cys
XM_017000823.2:c.15510G>C	XP_016856312.2:p.Trp5170Cys
XM_017000824.2:c.15456G>C	XP_016856313.2:p.Trp5152Cys
XM_017000825.2:c.15441G>C	XP_016856314.2:p.Trp5147Cys
XM_017000826.2:c.15438G>C	XP_016856315.2:p.Trp5146Cys
XM_017000827.2:c.15423G>C	XP_016856316.2:p.Trp5141Cys
XM_017000828.2:c.15399G>C	XP_016856317.2:p.Trp5133Cys
XM_017000829.2:c.15351G>C	XP_016856318.2:p.Trp5117Cys
XM_017000830.2:c.15300G>C	XP_016856319.2:p.Trp5100Cys
NM_020765.3:c.15291G>C MANE Select	NP_065816.2:p.Trp5097Cys