Canonical Allele Identifier: CA338748209

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404520A>G (hg19) ; chr1:g.19078026A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19078026A>G , CM000663.2:g.19078026A>G	GRCh38
NC_000001.10:g.19404520A>G , CM000663.1:g.19404520A>G	GRCh37
NC_000001.9:g.19277107A>G	NCBI36
NG_027669.1:g.137227T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15274T>C MANE Select	ENSP00000364403.3:p.Ser5092Pro
ENST00000375224.1:c.2395T>C	ENSP00000364372.1:p.Ser799Pro
ENST00000375225.7:c.499T>C	ENSP00000364373.3:p.Ser167Pro
ENST00000375254.7:c.15274T>C	ENSP00000364403.3:p.Ser5092Pro
ENST00000459947.5:n.3281T>C
NM_020765.2:c.15274T>C	NP_065816.2:p.Ser5092Pro
XM_011541108.1:c.15427T>C	XP_011539410.1:p.Ser5143Pro
XM_011541109.1:c.15424T>C	XP_011539411.1:p.Ser5142Pro
XM_011541110.1:c.15424T>C	XP_011539412.1:p.Ser5142Pro
XM_011541111.1:c.15424T>C	XP_011539413.1:p.Ser5142Pro
XM_011541112.1:c.15412T>C	XP_011539414.1:p.Ser5138Pro
XM_011541113.1:c.15409T>C	XP_011539415.1:p.Ser5137Pro
XM_011541114.1:c.15409T>C	XP_011539416.1:p.Ser5137Pro
XM_011541115.1:c.15403T>C	XP_011539417.1:p.Ser5135Pro
XM_011541116.1:c.15394T>C	XP_011539418.1:p.Ser5132Pro
XM_011541117.1:c.15343T>C	XP_011539419.1:p.Ser5115Pro
XM_011541118.1:c.15340T>C	XP_011539420.1:p.Ser5114Pro
XM_011541119.1:c.15307T>C	XP_011539421.1:p.Ser5103Pro
XM_011541120.1:c.15304T>C	XP_011539422.1:p.Ser5102Pro
XM_011541121.1:c.15271T>C	XP_011539423.1:p.Ser5091Pro
XM_011541108.3:c.15541T>C	XP_011539410.2:p.Ser5181Pro
XM_011541109.3:c.15538T>C	XP_011539411.2:p.Ser5180Pro
XM_011541110.3:c.15538T>C	XP_011539412.2:p.Ser5180Pro
XM_011541111.3:c.15538T>C	XP_011539413.2:p.Ser5180Pro
XM_011541112.3:c.15526T>C	XP_011539414.2:p.Ser5176Pro
XM_011541113.3:c.15523T>C	XP_011539415.2:p.Ser5175Pro
XM_011541114.3:c.15523T>C	XP_011539416.2:p.Ser5175Pro
XM_011541115.3:c.15517T>C	XP_011539417.2:p.Ser5173Pro
XM_011541116.3:c.15508T>C	XP_011539418.2:p.Ser5170Pro
XM_011541117.3:c.15457T>C	XP_011539419.2:p.Ser5153Pro
XM_011541118.3:c.15454T>C	XP_011539420.2:p.Ser5152Pro
XM_011541119.3:c.15421T>C	XP_011539421.2:p.Ser5141Pro
XM_011541120.3:c.15418T>C	XP_011539422.2:p.Ser5140Pro
XM_011541121.3:c.15385T>C	XP_011539423.2:p.Ser5129Pro
XM_017000822.2:c.15520T>C	XP_016856311.2:p.Ser5174Pro
XM_017000823.2:c.15493T>C	XP_016856312.2:p.Ser5165Pro
XM_017000824.2:c.15439T>C	XP_016856313.2:p.Ser5147Pro
XM_017000825.2:c.15424T>C	XP_016856314.2:p.Ser5142Pro
XM_017000826.2:c.15421T>C	XP_016856315.2:p.Ser5141Pro
XM_017000827.2:c.15406T>C	XP_016856316.2:p.Ser5136Pro
XM_017000828.2:c.15382T>C	XP_016856317.2:p.Ser5128Pro
XM_017000829.2:c.15334T>C	XP_016856318.2:p.Ser5112Pro
XM_017000830.2:c.15283T>C	XP_016856319.2:p.Ser5095Pro
NM_020765.3:c.15274T>C MANE Select	NP_065816.2:p.Ser5092Pro