Canonical Allele Identifier: CA416453041

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404488G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19077994G>A , CM000663.2:g.19077994G>A	GRCh38
NC_000001.10:g.19404488G>A , CM000663.1:g.19404488G>A	GRCh37
NC_000001.9:g.19277075G>A	NCBI36
NG_027669.1:g.137259C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15306C>T MANE Select	ENSP00000364403.3:p.Leu5102=
ENST00000375224.1:c.2427C>T	ENSP00000364372.1:p.Leu809=
ENST00000375225.7:c.531C>T	ENSP00000364373.3:p.Leu177=
ENST00000375254.7:c.15306C>T	ENSP00000364403.3:p.Leu5102=
ENST00000459947.5:n.3313C>T
NM_020765.2:c.15306C>T	NP_065816.2:p.Leu5102=
XM_011541108.1:c.15459C>T	XP_011539410.1:p.Leu5153=
XM_011541109.1:c.15456C>T	XP_011539411.1:p.Leu5152=
XM_011541110.1:c.15456C>T	XP_011539412.1:p.Leu5152=
XM_011541111.1:c.15456C>T	XP_011539413.1:p.Leu5152=
XM_011541112.1:c.15444C>T	XP_011539414.1:p.Leu5148=
XM_011541113.1:c.15441C>T	XP_011539415.1:p.Leu5147=
XM_011541114.1:c.15441C>T	XP_011539416.1:p.Leu5147=
XM_011541115.1:c.15435C>T	XP_011539417.1:p.Leu5145=
XM_011541116.1:c.15426C>T	XP_011539418.1:p.Leu5142=
XM_011541117.1:c.15375C>T	XP_011539419.1:p.Leu5125=
XM_011541118.1:c.15372C>T	XP_011539420.1:p.Leu5124=
XM_011541119.1:c.15339C>T	XP_011539421.1:p.Leu5113=
XM_011541120.1:c.15336C>T	XP_011539422.1:p.Leu5112=
XM_011541121.1:c.15303C>T	XP_011539423.1:p.Leu5101=
XM_011541108.3:c.15573C>T	XP_011539410.2:p.Leu5191=
XM_011541109.3:c.15570C>T	XP_011539411.2:p.Leu5190=
XM_011541110.3:c.15570C>T	XP_011539412.2:p.Leu5190=
XM_011541111.3:c.15570C>T	XP_011539413.2:p.Leu5190=
XM_011541112.3:c.15558C>T	XP_011539414.2:p.Leu5186=
XM_011541113.3:c.15555C>T	XP_011539415.2:p.Leu5185=
XM_011541114.3:c.15555C>T	XP_011539416.2:p.Leu5185=
XM_011541115.3:c.15549C>T	XP_011539417.2:p.Leu5183=
XM_011541116.3:c.15540C>T	XP_011539418.2:p.Leu5180=
XM_011541117.3:c.15489C>T	XP_011539419.2:p.Leu5163=
XM_011541118.3:c.15486C>T	XP_011539420.2:p.Leu5162=
XM_011541119.3:c.15453C>T	XP_011539421.2:p.Leu5151=
XM_011541120.3:c.15450C>T	XP_011539422.2:p.Leu5150=
XM_011541121.3:c.15417C>T	XP_011539423.2:p.Leu5139=
XM_017000822.2:c.15552C>T	XP_016856311.2:p.Leu5184=
XM_017000823.2:c.15525C>T	XP_016856312.2:p.Leu5175=
XM_017000824.2:c.15471C>T	XP_016856313.2:p.Leu5157=
XM_017000825.2:c.15456C>T	XP_016856314.2:p.Leu5152=
XM_017000826.2:c.15453C>T	XP_016856315.2:p.Leu5151=
XM_017000827.2:c.15438C>T	XP_016856316.2:p.Leu5146=
XM_017000828.2:c.15414C>T	XP_016856317.2:p.Leu5138=
XM_017000829.2:c.15366C>T	XP_016856318.2:p.Leu5122=
XM_017000830.2:c.15315C>T	XP_016856319.2:p.Leu5105=
NM_020765.3:c.15306C>T MANE Select	NP_065816.2:p.Leu5102=