Canonical Allele Identifier: CA338748053

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404475A>G (hg19) ; chr1:g.19077981A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19077981A>G , CM000663.2:g.19077981A>G	GRCh38
NC_000001.10:g.19404475A>G , CM000663.1:g.19404475A>G	GRCh37
NC_000001.9:g.19277062A>G	NCBI36
NG_027669.1:g.137272T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15319T>C MANE Select	ENSP00000364403.3:p.Phe5107Leu
ENST00000375224.1:c.2440T>C	ENSP00000364372.1:p.Phe814Leu
ENST00000375225.7:c.544T>C	ENSP00000364373.3:p.Phe182Leu
ENST00000375254.7:c.15319T>C	ENSP00000364403.3:p.Phe5107Leu
ENST00000459947.5:n.3326T>C
NM_020765.2:c.15319T>C	NP_065816.2:p.Phe5107Leu
XM_011541108.1:c.15472T>C	XP_011539410.1:p.Phe5158Leu
XM_011541109.1:c.15469T>C	XP_011539411.1:p.Phe5157Leu
XM_011541110.1:c.15469T>C	XP_011539412.1:p.Phe5157Leu
XM_011541111.1:c.15469T>C	XP_011539413.1:p.Phe5157Leu
XM_011541112.1:c.15457T>C	XP_011539414.1:p.Phe5153Leu
XM_011541113.1:c.15454T>C	XP_011539415.1:p.Phe5152Leu
XM_011541114.1:c.15454T>C	XP_011539416.1:p.Phe5152Leu
XM_011541115.1:c.15448T>C	XP_011539417.1:p.Phe5150Leu
XM_011541116.1:c.15439T>C	XP_011539418.1:p.Phe5147Leu
XM_011541117.1:c.15388T>C	XP_011539419.1:p.Phe5130Leu
XM_011541118.1:c.15385T>C	XP_011539420.1:p.Phe5129Leu
XM_011541119.1:c.15352T>C	XP_011539421.1:p.Phe5118Leu
XM_011541120.1:c.15349T>C	XP_011539422.1:p.Phe5117Leu
XM_011541121.1:c.15316T>C	XP_011539423.1:p.Phe5106Leu
XM_011541108.3:c.15586T>C	XP_011539410.2:p.Phe5196Leu
XM_011541109.3:c.15583T>C	XP_011539411.2:p.Phe5195Leu
XM_011541110.3:c.15583T>C	XP_011539412.2:p.Phe5195Leu
XM_011541111.3:c.15583T>C	XP_011539413.2:p.Phe5195Leu
XM_011541112.3:c.15571T>C	XP_011539414.2:p.Phe5191Leu
XM_011541113.3:c.15568T>C	XP_011539415.2:p.Phe5190Leu
XM_011541114.3:c.15568T>C	XP_011539416.2:p.Phe5190Leu
XM_011541115.3:c.15562T>C	XP_011539417.2:p.Phe5188Leu
XM_011541116.3:c.15553T>C	XP_011539418.2:p.Phe5185Leu
XM_011541117.3:c.15502T>C	XP_011539419.2:p.Phe5168Leu
XM_011541118.3:c.15499T>C	XP_011539420.2:p.Phe5167Leu
XM_011541119.3:c.15466T>C	XP_011539421.2:p.Phe5156Leu
XM_011541120.3:c.15463T>C	XP_011539422.2:p.Phe5155Leu
XM_011541121.3:c.15430T>C	XP_011539423.2:p.Phe5144Leu
XM_017000822.2:c.15565T>C	XP_016856311.2:p.Phe5189Leu
XM_017000823.2:c.15538T>C	XP_016856312.2:p.Phe5180Leu
XM_017000824.2:c.15484T>C	XP_016856313.2:p.Phe5162Leu
XM_017000825.2:c.15469T>C	XP_016856314.2:p.Phe5157Leu
XM_017000826.2:c.15466T>C	XP_016856315.2:p.Phe5156Leu
XM_017000827.2:c.15451T>C	XP_016856316.2:p.Phe5151Leu
XM_017000828.2:c.15427T>C	XP_016856317.2:p.Phe5143Leu
XM_017000829.2:c.15379T>C	XP_016856318.2:p.Phe5127Leu
XM_017000830.2:c.15328T>C	XP_016856319.2:p.Phe5110Leu
NM_020765.3:c.15319T>C MANE Select	NP_065816.2:p.Phe5107Leu