Canonical Allele Identifier: CA416452962

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404470C>T (hg19)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15324G>A MANE Select	ENSP00000364403.3:p.Lys5108=
ENST00000375224.1:c.2445G>A	ENSP00000364372.1:p.Lys815=
ENST00000375225.7:c.549G>A	ENSP00000364373.3:p.Lys183=
ENST00000375254.7:c.15324G>A	ENSP00000364403.3:p.Lys5108=
ENST00000459947.5:n.3331G>A
NM_020765.2:c.15324G>A	NP_065816.2:p.Lys5108=
XM_011541108.1:c.15477G>A	XP_011539410.1:p.Lys5159=
XM_011541109.1:c.15474G>A	XP_011539411.1:p.Lys5158=
XM_011541110.1:c.15474G>A	XP_011539412.1:p.Lys5158=
XM_011541111.1:c.15474G>A	XP_011539413.1:p.Lys5158=
XM_011541112.1:c.15462G>A	XP_011539414.1:p.Lys5154=
XM_011541113.1:c.15459G>A	XP_011539415.1:p.Lys5153=
XM_011541114.1:c.15459G>A	XP_011539416.1:p.Lys5153=
XM_011541115.1:c.15453G>A	XP_011539417.1:p.Lys5151=
XM_011541116.1:c.15444G>A	XP_011539418.1:p.Lys5148=
XM_011541117.1:c.15393G>A	XP_011539419.1:p.Lys5131=
XM_011541118.1:c.15390G>A	XP_011539420.1:p.Lys5130=
XM_011541119.1:c.15357G>A	XP_011539421.1:p.Lys5119=
XM_011541120.1:c.15354G>A	XP_011539422.1:p.Lys5118=
XM_011541121.1:c.15321G>A	XP_011539423.1:p.Lys5107=
XM_011541108.3:c.15591G>A	XP_011539410.2:p.Lys5197=
XM_011541109.3:c.15588G>A	XP_011539411.2:p.Lys5196=
XM_011541110.3:c.15588G>A	XP_011539412.2:p.Lys5196=
XM_011541111.3:c.15588G>A	XP_011539413.2:p.Lys5196=
XM_011541112.3:c.15576G>A	XP_011539414.2:p.Lys5192=
XM_011541113.3:c.15573G>A	XP_011539415.2:p.Lys5191=
XM_011541114.3:c.15573G>A	XP_011539416.2:p.Lys5191=
XM_011541115.3:c.15567G>A	XP_011539417.2:p.Lys5189=
XM_011541116.3:c.15558G>A	XP_011539418.2:p.Lys5186=
XM_011541117.3:c.15507G>A	XP_011539419.2:p.Lys5169=
XM_011541118.3:c.15504G>A	XP_011539420.2:p.Lys5168=
XM_011541119.3:c.15471G>A	XP_011539421.2:p.Lys5157=
XM_011541120.3:c.15468G>A	XP_011539422.2:p.Lys5156=
XM_011541121.3:c.15435G>A	XP_011539423.2:p.Lys5145=
XM_017000822.2:c.15570G>A	XP_016856311.2:p.Lys5190=
XM_017000823.2:c.15543G>A	XP_016856312.2:p.Lys5181=
XM_017000824.2:c.15489G>A	XP_016856313.2:p.Lys5163=
XM_017000825.2:c.15474G>A	XP_016856314.2:p.Lys5158=
XM_017000826.2:c.15471G>A	XP_016856315.2:p.Lys5157=
XM_017000827.2:c.15456G>A	XP_016856316.2:p.Lys5152=
XM_017000828.2:c.15432G>A	XP_016856317.2:p.Lys5144=
XM_017000829.2:c.15384G>A	XP_016856318.2:p.Lys5128=
XM_017000830.2:c.15333G>A	XP_016856319.2:p.Lys5111=
NM_020765.3:c.15324G>A MANE Select	NP_065816.2:p.Lys5108=