Canonical Allele Identifier: CA338748055

Gene: UBR4

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15319T>A MANE Select	ENSP00000364403.3:p.Phe5107Ile
ENST00000375224.1:c.2440T>A	ENSP00000364372.1:p.Phe814Ile
ENST00000375225.7:c.544T>A	ENSP00000364373.3:p.Phe182Ile
ENST00000375254.7:c.15319T>A	ENSP00000364403.3:p.Phe5107Ile
ENST00000459947.5:n.3326T>A
NM_020765.2:c.15319T>A	NP_065816.2:p.Phe5107Ile
XM_011541108.1:c.15472T>A	XP_011539410.1:p.Phe5158Ile
XM_011541109.1:c.15469T>A	XP_011539411.1:p.Phe5157Ile
XM_011541110.1:c.15469T>A	XP_011539412.1:p.Phe5157Ile
XM_011541111.1:c.15469T>A	XP_011539413.1:p.Phe5157Ile
XM_011541112.1:c.15457T>A	XP_011539414.1:p.Phe5153Ile
XM_011541113.1:c.15454T>A	XP_011539415.1:p.Phe5152Ile
XM_011541114.1:c.15454T>A	XP_011539416.1:p.Phe5152Ile
XM_011541115.1:c.15448T>A	XP_011539417.1:p.Phe5150Ile
XM_011541116.1:c.15439T>A	XP_011539418.1:p.Phe5147Ile
XM_011541117.1:c.15388T>A	XP_011539419.1:p.Phe5130Ile
XM_011541118.1:c.15385T>A	XP_011539420.1:p.Phe5129Ile
XM_011541119.1:c.15352T>A	XP_011539421.1:p.Phe5118Ile
XM_011541120.1:c.15349T>A	XP_011539422.1:p.Phe5117Ile
XM_011541121.1:c.15316T>A	XP_011539423.1:p.Phe5106Ile
XM_011541108.3:c.15586T>A	XP_011539410.2:p.Phe5196Ile
XM_011541109.3:c.15583T>A	XP_011539411.2:p.Phe5195Ile
XM_011541110.3:c.15583T>A	XP_011539412.2:p.Phe5195Ile
XM_011541111.3:c.15583T>A	XP_011539413.2:p.Phe5195Ile
XM_011541112.3:c.15571T>A	XP_011539414.2:p.Phe5191Ile
XM_011541113.3:c.15568T>A	XP_011539415.2:p.Phe5190Ile
XM_011541114.3:c.15568T>A	XP_011539416.2:p.Phe5190Ile
XM_011541115.3:c.15562T>A	XP_011539417.2:p.Phe5188Ile
XM_011541116.3:c.15553T>A	XP_011539418.2:p.Phe5185Ile
XM_011541117.3:c.15502T>A	XP_011539419.2:p.Phe5168Ile
XM_011541118.3:c.15499T>A	XP_011539420.2:p.Phe5167Ile
XM_011541119.3:c.15466T>A	XP_011539421.2:p.Phe5156Ile
XM_011541120.3:c.15463T>A	XP_011539422.2:p.Phe5155Ile
XM_011541121.3:c.15430T>A	XP_011539423.2:p.Phe5144Ile
XM_017000822.2:c.15565T>A	XP_016856311.2:p.Phe5189Ile
XM_017000823.2:c.15538T>A	XP_016856312.2:p.Phe5180Ile
XM_017000824.2:c.15484T>A	XP_016856313.2:p.Phe5162Ile
XM_017000825.2:c.15469T>A	XP_016856314.2:p.Phe5157Ile
XM_017000826.2:c.15466T>A	XP_016856315.2:p.Phe5156Ile
XM_017000827.2:c.15451T>A	XP_016856316.2:p.Phe5151Ile
XM_017000828.2:c.15427T>A	XP_016856317.2:p.Phe5143Ile
XM_017000829.2:c.15379T>A	XP_016856318.2:p.Phe5127Ile
XM_017000830.2:c.15328T>A	XP_016856319.2:p.Phe5110Ile
NM_020765.3:c.15319T>A MANE Select	NP_065816.2:p.Phe5107Ile