Canonical Allele Identifier: CA338748041

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404473A>C (hg19) ; chr1:g.19077979A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19077979A>C , CM000663.2:g.19077979A>C	GRCh38
NC_000001.10:g.19404473A>C , CM000663.1:g.19404473A>C	GRCh37
NC_000001.9:g.19277060A>C	NCBI36
NG_027669.1:g.137274T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15321T>G MANE Select	ENSP00000364403.3:p.Phe5107Leu
ENST00000375224.1:c.2442T>G	ENSP00000364372.1:p.Phe814Leu
ENST00000375225.7:c.546T>G	ENSP00000364373.3:p.Phe182Leu
ENST00000375254.7:c.15321T>G	ENSP00000364403.3:p.Phe5107Leu
ENST00000459947.5:n.3328T>G
NM_020765.2:c.15321T>G	NP_065816.2:p.Phe5107Leu
XM_011541108.1:c.15474T>G	XP_011539410.1:p.Phe5158Leu
XM_011541109.1:c.15471T>G	XP_011539411.1:p.Phe5157Leu
XM_011541110.1:c.15471T>G	XP_011539412.1:p.Phe5157Leu
XM_011541111.1:c.15471T>G	XP_011539413.1:p.Phe5157Leu
XM_011541112.1:c.15459T>G	XP_011539414.1:p.Phe5153Leu
XM_011541113.1:c.15456T>G	XP_011539415.1:p.Phe5152Leu
XM_011541114.1:c.15456T>G	XP_011539416.1:p.Phe5152Leu
XM_011541115.1:c.15450T>G	XP_011539417.1:p.Phe5150Leu
XM_011541116.1:c.15441T>G	XP_011539418.1:p.Phe5147Leu
XM_011541117.1:c.15390T>G	XP_011539419.1:p.Phe5130Leu
XM_011541118.1:c.15387T>G	XP_011539420.1:p.Phe5129Leu
XM_011541119.1:c.15354T>G	XP_011539421.1:p.Phe5118Leu
XM_011541120.1:c.15351T>G	XP_011539422.1:p.Phe5117Leu
XM_011541121.1:c.15318T>G	XP_011539423.1:p.Phe5106Leu
XM_011541108.3:c.15588T>G	XP_011539410.2:p.Phe5196Leu
XM_011541109.3:c.15585T>G	XP_011539411.2:p.Phe5195Leu
XM_011541110.3:c.15585T>G	XP_011539412.2:p.Phe5195Leu
XM_011541111.3:c.15585T>G	XP_011539413.2:p.Phe5195Leu
XM_011541112.3:c.15573T>G	XP_011539414.2:p.Phe5191Leu
XM_011541113.3:c.15570T>G	XP_011539415.2:p.Phe5190Leu
XM_011541114.3:c.15570T>G	XP_011539416.2:p.Phe5190Leu
XM_011541115.3:c.15564T>G	XP_011539417.2:p.Phe5188Leu
XM_011541116.3:c.15555T>G	XP_011539418.2:p.Phe5185Leu
XM_011541117.3:c.15504T>G	XP_011539419.2:p.Phe5168Leu
XM_011541118.3:c.15501T>G	XP_011539420.2:p.Phe5167Leu
XM_011541119.3:c.15468T>G	XP_011539421.2:p.Phe5156Leu
XM_011541120.3:c.15465T>G	XP_011539422.2:p.Phe5155Leu
XM_011541121.3:c.15432T>G	XP_011539423.2:p.Phe5144Leu
XM_017000822.2:c.15567T>G	XP_016856311.2:p.Phe5189Leu
XM_017000823.2:c.15540T>G	XP_016856312.2:p.Phe5180Leu
XM_017000824.2:c.15486T>G	XP_016856313.2:p.Phe5162Leu
XM_017000825.2:c.15471T>G	XP_016856314.2:p.Phe5157Leu
XM_017000826.2:c.15468T>G	XP_016856315.2:p.Phe5156Leu
XM_017000827.2:c.15453T>G	XP_016856316.2:p.Phe5151Leu
XM_017000828.2:c.15429T>G	XP_016856317.2:p.Phe5143Leu
XM_017000829.2:c.15381T>G	XP_016856318.2:p.Phe5127Leu
XM_017000830.2:c.15330T>G	XP_016856319.2:p.Phe5110Leu
NM_020765.3:c.15321T>G MANE Select	NP_065816.2:p.Phe5107Leu