Canonical Allele Identifier: CA338748049
Gene: UBR4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.19077980A>C , CM000663.2:g.19077980A>C GRCh38
NC_000001.10:g.19404474A>C , CM000663.1:g.19404474A>C GRCh37
NC_000001.9:g.19277061A>C NCBI36
NG_027669.1:g.137273T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375254.8:c.15320T>G MANE Select ENSP00000364403.3:p.Phe5107Cys
ENST00000375224.1:c.2441T>G ENSP00000364372.1:p.Phe814Cys
ENST00000375225.7:c.545T>G ENSP00000364373.3:p.Phe182Cys
ENST00000375254.7:c.15320T>G ENSP00000364403.3:p.Phe5107Cys
ENST00000459947.5:n.3327T>G
NM_020765.2:c.15320T>G NP_065816.2:p.Phe5107Cys
XM_011541108.1:c.15473T>G XP_011539410.1:p.Phe5158Cys
XM_011541109.1:c.15470T>G XP_011539411.1:p.Phe5157Cys
XM_011541110.1:c.15470T>G XP_011539412.1:p.Phe5157Cys
XM_011541111.1:c.15470T>G XP_011539413.1:p.Phe5157Cys
XM_011541112.1:c.15458T>G XP_011539414.1:p.Phe5153Cys
XM_011541113.1:c.15455T>G XP_011539415.1:p.Phe5152Cys
XM_011541114.1:c.15455T>G XP_011539416.1:p.Phe5152Cys
XM_011541115.1:c.15449T>G XP_011539417.1:p.Phe5150Cys
XM_011541116.1:c.15440T>G XP_011539418.1:p.Phe5147Cys
XM_011541117.1:c.15389T>G XP_011539419.1:p.Phe5130Cys
XM_011541118.1:c.15386T>G XP_011539420.1:p.Phe5129Cys
XM_011541119.1:c.15353T>G XP_011539421.1:p.Phe5118Cys
XM_011541120.1:c.15350T>G XP_011539422.1:p.Phe5117Cys
XM_011541121.1:c.15317T>G XP_011539423.1:p.Phe5106Cys
XM_011541108.3:c.15587T>G XP_011539410.2:p.Phe5196Cys
XM_011541109.3:c.15584T>G XP_011539411.2:p.Phe5195Cys
XM_011541110.3:c.15584T>G XP_011539412.2:p.Phe5195Cys
XM_011541111.3:c.15584T>G XP_011539413.2:p.Phe5195Cys
XM_011541112.3:c.15572T>G XP_011539414.2:p.Phe5191Cys
XM_011541113.3:c.15569T>G XP_011539415.2:p.Phe5190Cys
XM_011541114.3:c.15569T>G XP_011539416.2:p.Phe5190Cys
XM_011541115.3:c.15563T>G XP_011539417.2:p.Phe5188Cys
XM_011541116.3:c.15554T>G XP_011539418.2:p.Phe5185Cys
XM_011541117.3:c.15503T>G XP_011539419.2:p.Phe5168Cys
XM_011541118.3:c.15500T>G XP_011539420.2:p.Phe5167Cys
XM_011541119.3:c.15467T>G XP_011539421.2:p.Phe5156Cys
XM_011541120.3:c.15464T>G XP_011539422.2:p.Phe5155Cys
XM_011541121.3:c.15431T>G XP_011539423.2:p.Phe5144Cys
XM_017000822.2:c.15566T>G XP_016856311.2:p.Phe5189Cys
XM_017000823.2:c.15539T>G XP_016856312.2:p.Phe5180Cys
XM_017000824.2:c.15485T>G XP_016856313.2:p.Phe5162Cys
XM_017000825.2:c.15470T>G XP_016856314.2:p.Phe5157Cys
XM_017000826.2:c.15467T>G XP_016856315.2:p.Phe5156Cys
XM_017000827.2:c.15452T>G XP_016856316.2:p.Phe5151Cys
XM_017000828.2:c.15428T>G XP_016856317.2:p.Phe5143Cys
XM_017000829.2:c.15380T>G XP_016856318.2:p.Phe5127Cys
XM_017000830.2:c.15329T>G XP_016856319.2:p.Phe5110Cys
NM_020765.3:c.15320T>G MANE Select NP_065816.2:p.Phe5107Cys