Canonical Allele Identifier: CA999227634

Gene: UBR4

Linked Data

• dbSNP Id: rs763524091
• gnomAD v3: 1-19077762-A-AAACCAAACC
• gnomAD v4: 1-19077762-A-AAACCAAACC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19077764_19077765insCCAAACCAA , CM000663.2:g.19077764_19077765insCCAAACCAA	GRCh38
NC_000001.10:g.19404258_19404259insCCAAACCAA , CM000663.1:g.19404258_19404259insCCAAACCAA	GRCh37
NC_000001.9:g.19276845_19276846insCCAAACCAA	NCBI36
NG_027669.1:g.137490_137491insGGTTTGGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15324+213_15324+214insGGTTTGGTT MANE Select	ENSP00000364403.3:n.15324+213_15324+214insGGTTTGGTT
ENST00000375224.1:c.2445+213_2445+214insGGTTTGGTT	ENSP00000364372.1:n.2445+213_2445+214insGGTTTGGTT
ENST00000375225.7:c.549+213_549+214insGGTTTGGTT	ENSP00000364373.3:n.549+213_549+214insGGTTTGGTT
ENST00000375254.7:c.15324+213_15324+214insGGTTTGGTT	ENSP00000364403.3:n.15324+213_15324+214insGGTTTGGTT
ENST00000459947.5:n.3331+213_3331+214insGGTTTGGTT
ENST00000486515.1:n.43+22_43+23insGGTTTGGTT
NM_020765.2:c.15324+213_15324+214insGGTTTGGTT	NP_065816.2:n.15324+213_15324+214insGGTTTGGTT
XM_011541108.1:c.15477+213_15477+214insGGTTTGGTT	XP_011539410.1:n.15477+213_15477+214insGGTTTGGTT
XM_011541109.1:c.15474+213_15474+214insGGTTTGGTT	XP_011539411.1:n.15474+213_15474+214insGGTTTGGTT
XM_011541110.1:c.15474+213_15474+214insGGTTTGGTT	XP_011539412.1:n.15474+213_15474+214insGGTTTGGTT
XM_011541111.1:c.15474+213_15474+214insGGTTTGGTT	XP_011539413.1:n.15474+213_15474+214insGGTTTGGTT
XM_011541112.1:c.15462+213_15462+214insGGTTTGGTT	XP_011539414.1:n.15462+213_15462+214insGGTTTGGTT
XM_011541113.1:c.15459+213_15459+214insGGTTTGGTT	XP_011539415.1:n.15459+213_15459+214insGGTTTGGTT
XM_011541114.1:c.15459+213_15459+214insGGTTTGGTT	XP_011539416.1:n.15459+213_15459+214insGGTTTGGTT
XM_011541115.1:c.15453+213_15453+214insGGTTTGGTT	XP_011539417.1:n.15453+213_15453+214insGGTTTGGTT
XM_011541116.1:c.15444+213_15444+214insGGTTTGGTT	XP_011539418.1:n.15444+213_15444+214insGGTTTGGTT
XM_011541117.1:c.15393+213_15393+214insGGTTTGGTT	XP_011539419.1:n.15393+213_15393+214insGGTTTGGTT
XM_011541118.1:c.15390+213_15390+214insGGTTTGGTT	XP_011539420.1:n.15390+213_15390+214insGGTTTGGTT
XM_011541119.1:c.15357+213_15357+214insGGTTTGGTT	XP_011539421.1:n.15357+213_15357+214insGGTTTGGTT
XM_011541120.1:c.15354+213_15354+214insGGTTTGGTT	XP_011539422.1:n.15354+213_15354+214insGGTTTGGTT
XM_011541121.1:c.15321+213_15321+214insGGTTTGGTT	XP_011539423.1:n.15321+213_15321+214insGGTTTGGTT
XM_011541108.3:c.15591+213_15591+214insGGTTTGGTT	XP_011539410.2:n.15591+213_15591+214insGGTTTGGTT
XM_011541109.3:c.15588+213_15588+214insGGTTTGGTT	XP_011539411.2:n.15588+213_15588+214insGGTTTGGTT
XM_011541110.3:c.15588+213_15588+214insGGTTTGGTT	XP_011539412.2:n.15588+213_15588+214insGGTTTGGTT
XM_011541111.3:c.15588+213_15588+214insGGTTTGGTT	XP_011539413.2:n.15588+213_15588+214insGGTTTGGTT
XM_011541112.3:c.15576+213_15576+214insGGTTTGGTT	XP_011539414.2:n.15576+213_15576+214insGGTTTGGTT
XM_011541113.3:c.15573+213_15573+214insGGTTTGGTT	XP_011539415.2:n.15573+213_15573+214insGGTTTGGTT
XM_011541114.3:c.15573+213_15573+214insGGTTTGGTT	XP_011539416.2:n.15573+213_15573+214insGGTTTGGTT
XM_011541115.3:c.15567+213_15567+214insGGTTTGGTT	XP_011539417.2:n.15567+213_15567+214insGGTTTGGTT
XM_011541116.3:c.15558+213_15558+214insGGTTTGGTT	XP_011539418.2:n.15558+213_15558+214insGGTTTGGTT
XM_011541117.3:c.15507+213_15507+214insGGTTTGGTT	XP_011539419.2:n.15507+213_15507+214insGGTTTGGTT
XM_011541118.3:c.15504+213_15504+214insGGTTTGGTT	XP_011539420.2:n.15504+213_15504+214insGGTTTGGTT
XM_011541119.3:c.15471+213_15471+214insGGTTTGGTT	XP_011539421.2:n.15471+213_15471+214insGGTTTGGTT
XM_011541120.3:c.15468+213_15468+214insGGTTTGGTT	XP_011539422.2:n.15468+213_15468+214insGGTTTGGTT
XM_011541121.3:c.15435+213_15435+214insGGTTTGGTT	XP_011539423.2:n.15435+213_15435+214insGGTTTGGTT
XM_017000822.2:c.15570+213_15570+214insGGTTTGGTT	XP_016856311.2:n.15570+213_15570+214insGGTTTGGTT
XM_017000823.2:c.15543+213_15543+214insGGTTTGGTT	XP_016856312.2:n.15543+213_15543+214insGGTTTGGTT
XM_017000824.2:c.15489+213_15489+214insGGTTTGGTT	XP_016856313.2:n.15489+213_15489+214insGGTTTGGTT
XM_017000825.2:c.15474+213_15474+214insGGTTTGGTT	XP_016856314.2:n.15474+213_15474+214insGGTTTGGTT
XM_017000826.2:c.15471+213_15471+214insGGTTTGGTT	XP_016856315.2:n.15471+213_15471+214insGGTTTGGTT
XM_017000827.2:c.15456+213_15456+214insGGTTTGGTT	XP_016856316.2:n.15456+213_15456+214insGGTTTGGTT
XM_017000828.2:c.15432+213_15432+214insGGTTTGGTT	XP_016856317.2:n.15432+213_15432+214insGGTTTGGTT
XM_017000829.2:c.15384+213_15384+214insGGTTTGGTT	XP_016856318.2:n.15384+213_15384+214insGGTTTGGTT
XM_017000830.2:c.15333+213_15333+214insGGTTTGGTT	XP_016856319.2:n.15333+213_15333+214insGGTTTGGTT
NM_020765.3:c.15324+213_15324+214insGGTTTGGTT MANE Select	NP_065816.2:n.15324+213_15324+214insGGTTTGGTT