Canonical Allele Identifier: CA338748027

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404470C>G (hg19) ; chr1:g.19077976C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19077976C>G , CM000663.2:g.19077976C>G	GRCh38
NC_000001.10:g.19404470C>G , CM000663.1:g.19404470C>G	GRCh37
NC_000001.9:g.19277057C>G	NCBI36
NG_027669.1:g.137277G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15324G>C MANE Select	ENSP00000364403.3:p.Lys5108Asn
ENST00000375224.1:c.2445G>C	ENSP00000364372.1:p.Lys815Asn
ENST00000375225.7:c.549G>C	ENSP00000364373.3:p.Lys183Asn
ENST00000375254.7:c.15324G>C	ENSP00000364403.3:p.Lys5108Asn
ENST00000459947.5:n.3331G>C
NM_020765.2:c.15324G>C	NP_065816.2:p.Lys5108Asn
XM_011541108.1:c.15477G>C	XP_011539410.1:p.Lys5159Asn
XM_011541109.1:c.15474G>C	XP_011539411.1:p.Lys5158Asn
XM_011541110.1:c.15474G>C	XP_011539412.1:p.Lys5158Asn
XM_011541111.1:c.15474G>C	XP_011539413.1:p.Lys5158Asn
XM_011541112.1:c.15462G>C	XP_011539414.1:p.Lys5154Asn
XM_011541113.1:c.15459G>C	XP_011539415.1:p.Lys5153Asn
XM_011541114.1:c.15459G>C	XP_011539416.1:p.Lys5153Asn
XM_011541115.1:c.15453G>C	XP_011539417.1:p.Lys5151Asn
XM_011541116.1:c.15444G>C	XP_011539418.1:p.Lys5148Asn
XM_011541117.1:c.15393G>C	XP_011539419.1:p.Lys5131Asn
XM_011541118.1:c.15390G>C	XP_011539420.1:p.Lys5130Asn
XM_011541119.1:c.15357G>C	XP_011539421.1:p.Lys5119Asn
XM_011541120.1:c.15354G>C	XP_011539422.1:p.Lys5118Asn
XM_011541121.1:c.15321G>C	XP_011539423.1:p.Lys5107Asn
XM_011541108.3:c.15591G>C	XP_011539410.2:p.Lys5197Asn
XM_011541109.3:c.15588G>C	XP_011539411.2:p.Lys5196Asn
XM_011541110.3:c.15588G>C	XP_011539412.2:p.Lys5196Asn
XM_011541111.3:c.15588G>C	XP_011539413.2:p.Lys5196Asn
XM_011541112.3:c.15576G>C	XP_011539414.2:p.Lys5192Asn
XM_011541113.3:c.15573G>C	XP_011539415.2:p.Lys5191Asn
XM_011541114.3:c.15573G>C	XP_011539416.2:p.Lys5191Asn
XM_011541115.3:c.15567G>C	XP_011539417.2:p.Lys5189Asn
XM_011541116.3:c.15558G>C	XP_011539418.2:p.Lys5186Asn
XM_011541117.3:c.15507G>C	XP_011539419.2:p.Lys5169Asn
XM_011541118.3:c.15504G>C	XP_011539420.2:p.Lys5168Asn
XM_011541119.3:c.15471G>C	XP_011539421.2:p.Lys5157Asn
XM_011541120.3:c.15468G>C	XP_011539422.2:p.Lys5156Asn
XM_011541121.3:c.15435G>C	XP_011539423.2:p.Lys5145Asn
XM_017000822.2:c.15570G>C	XP_016856311.2:p.Lys5190Asn
XM_017000823.2:c.15543G>C	XP_016856312.2:p.Lys5181Asn
XM_017000824.2:c.15489G>C	XP_016856313.2:p.Lys5163Asn
XM_017000825.2:c.15474G>C	XP_016856314.2:p.Lys5158Asn
XM_017000826.2:c.15471G>C	XP_016856315.2:p.Lys5157Asn
XM_017000827.2:c.15456G>C	XP_016856316.2:p.Lys5152Asn
XM_017000828.2:c.15432G>C	XP_016856317.2:p.Lys5144Asn
XM_017000829.2:c.15384G>C	XP_016856318.2:p.Lys5128Asn
XM_017000830.2:c.15333G>C	XP_016856319.2:p.Lys5111Asn
NM_020765.3:c.15324G>C MANE Select	NP_065816.2:p.Lys5108Asn