Canonical Allele Identifier: CA338748047

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404474A>G (hg19) ; chr1:g.19077980A>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15320T>C MANE Select	ENSP00000364403.3:p.Phe5107Ser
ENST00000375224.1:c.2441T>C	ENSP00000364372.1:p.Phe814Ser
ENST00000375225.7:c.545T>C	ENSP00000364373.3:p.Phe182Ser
ENST00000375254.7:c.15320T>C	ENSP00000364403.3:p.Phe5107Ser
ENST00000459947.5:n.3327T>C
NM_020765.2:c.15320T>C	NP_065816.2:p.Phe5107Ser
XM_011541108.1:c.15473T>C	XP_011539410.1:p.Phe5158Ser
XM_011541109.1:c.15470T>C	XP_011539411.1:p.Phe5157Ser
XM_011541110.1:c.15470T>C	XP_011539412.1:p.Phe5157Ser
XM_011541111.1:c.15470T>C	XP_011539413.1:p.Phe5157Ser
XM_011541112.1:c.15458T>C	XP_011539414.1:p.Phe5153Ser
XM_011541113.1:c.15455T>C	XP_011539415.1:p.Phe5152Ser
XM_011541114.1:c.15455T>C	XP_011539416.1:p.Phe5152Ser
XM_011541115.1:c.15449T>C	XP_011539417.1:p.Phe5150Ser
XM_011541116.1:c.15440T>C	XP_011539418.1:p.Phe5147Ser
XM_011541117.1:c.15389T>C	XP_011539419.1:p.Phe5130Ser
XM_011541118.1:c.15386T>C	XP_011539420.1:p.Phe5129Ser
XM_011541119.1:c.15353T>C	XP_011539421.1:p.Phe5118Ser
XM_011541120.1:c.15350T>C	XP_011539422.1:p.Phe5117Ser
XM_011541121.1:c.15317T>C	XP_011539423.1:p.Phe5106Ser
XM_011541108.3:c.15587T>C	XP_011539410.2:p.Phe5196Ser
XM_011541109.3:c.15584T>C	XP_011539411.2:p.Phe5195Ser
XM_011541110.3:c.15584T>C	XP_011539412.2:p.Phe5195Ser
XM_011541111.3:c.15584T>C	XP_011539413.2:p.Phe5195Ser
XM_011541112.3:c.15572T>C	XP_011539414.2:p.Phe5191Ser
XM_011541113.3:c.15569T>C	XP_011539415.2:p.Phe5190Ser
XM_011541114.3:c.15569T>C	XP_011539416.2:p.Phe5190Ser
XM_011541115.3:c.15563T>C	XP_011539417.2:p.Phe5188Ser
XM_011541116.3:c.15554T>C	XP_011539418.2:p.Phe5185Ser
XM_011541117.3:c.15503T>C	XP_011539419.2:p.Phe5168Ser
XM_011541118.3:c.15500T>C	XP_011539420.2:p.Phe5167Ser
XM_011541119.3:c.15467T>C	XP_011539421.2:p.Phe5156Ser
XM_011541120.3:c.15464T>C	XP_011539422.2:p.Phe5155Ser
XM_011541121.3:c.15431T>C	XP_011539423.2:p.Phe5144Ser
XM_017000822.2:c.15566T>C	XP_016856311.2:p.Phe5189Ser
XM_017000823.2:c.15539T>C	XP_016856312.2:p.Phe5180Ser
XM_017000824.2:c.15485T>C	XP_016856313.2:p.Phe5162Ser
XM_017000825.2:c.15470T>C	XP_016856314.2:p.Phe5157Ser
XM_017000826.2:c.15467T>C	XP_016856315.2:p.Phe5156Ser
XM_017000827.2:c.15452T>C	XP_016856316.2:p.Phe5151Ser
XM_017000828.2:c.15428T>C	XP_016856317.2:p.Phe5143Ser
XM_017000829.2:c.15380T>C	XP_016856318.2:p.Phe5127Ser
XM_017000830.2:c.15329T>C	XP_016856319.2:p.Phe5110Ser
NM_020765.3:c.15320T>C MANE Select	NP_065816.2:p.Phe5107Ser