Canonical Allele Identifier: CA338748018

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404468A>G (hg19) ; chr1:g.19077974A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19077974A>G , CM000663.2:g.19077974A>G	GRCh38
NC_000001.10:g.19404468A>G , CM000663.1:g.19404468A>G	GRCh37
NC_000001.9:g.19277055A>G	NCBI36
NG_027669.1:g.137279T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15324+2T>C MANE Select	ENSP00000364403.3:n.15324+2T>C
ENST00000375224.1:c.2445+2T>C	ENSP00000364372.1:n.2445+2T>C
ENST00000375225.7:c.549+2T>C	ENSP00000364373.3:n.549+2T>C
ENST00000375254.7:c.15324+2T>C	ENSP00000364403.3:n.15324+2T>C
ENST00000459947.5:n.3331+2T>C
NM_020765.2:c.15324+2T>C	NP_065816.2:n.15324+2T>C
XM_011541108.1:c.15477+2T>C	XP_011539410.1:n.15477+2T>C
XM_011541109.1:c.15474+2T>C	XP_011539411.1:n.15474+2T>C
XM_011541110.1:c.15474+2T>C	XP_011539412.1:n.15474+2T>C
XM_011541111.1:c.15474+2T>C	XP_011539413.1:n.15474+2T>C
XM_011541112.1:c.15462+2T>C	XP_011539414.1:n.15462+2T>C
XM_011541113.1:c.15459+2T>C	XP_011539415.1:n.15459+2T>C
XM_011541114.1:c.15459+2T>C	XP_011539416.1:n.15459+2T>C
XM_011541115.1:c.15453+2T>C	XP_011539417.1:n.15453+2T>C
XM_011541116.1:c.15444+2T>C	XP_011539418.1:n.15444+2T>C
XM_011541117.1:c.15393+2T>C	XP_011539419.1:n.15393+2T>C
XM_011541118.1:c.15390+2T>C	XP_011539420.1:n.15390+2T>C
XM_011541119.1:c.15357+2T>C	XP_011539421.1:n.15357+2T>C
XM_011541120.1:c.15354+2T>C	XP_011539422.1:n.15354+2T>C
XM_011541121.1:c.15321+2T>C	XP_011539423.1:n.15321+2T>C
XM_011541108.3:c.15591+2T>C	XP_011539410.2:n.15591+2T>C
XM_011541109.3:c.15588+2T>C	XP_011539411.2:n.15588+2T>C
XM_011541110.3:c.15588+2T>C	XP_011539412.2:n.15588+2T>C
XM_011541111.3:c.15588+2T>C	XP_011539413.2:n.15588+2T>C
XM_011541112.3:c.15576+2T>C	XP_011539414.2:n.15576+2T>C
XM_011541113.3:c.15573+2T>C	XP_011539415.2:n.15573+2T>C
XM_011541114.3:c.15573+2T>C	XP_011539416.2:n.15573+2T>C
XM_011541115.3:c.15567+2T>C	XP_011539417.2:n.15567+2T>C
XM_011541116.3:c.15558+2T>C	XP_011539418.2:n.15558+2T>C
XM_011541117.3:c.15507+2T>C	XP_011539419.2:n.15507+2T>C
XM_011541118.3:c.15504+2T>C	XP_011539420.2:n.15504+2T>C
XM_011541119.3:c.15471+2T>C	XP_011539421.2:n.15471+2T>C
XM_011541120.3:c.15468+2T>C	XP_011539422.2:n.15468+2T>C
XM_011541121.3:c.15435+2T>C	XP_011539423.2:n.15435+2T>C
XM_017000822.2:c.15570+2T>C	XP_016856311.2:n.15570+2T>C
XM_017000823.2:c.15543+2T>C	XP_016856312.2:n.15543+2T>C
XM_017000824.2:c.15489+2T>C	XP_016856313.2:n.15489+2T>C
XM_017000825.2:c.15474+2T>C	XP_016856314.2:n.15474+2T>C
XM_017000826.2:c.15471+2T>C	XP_016856315.2:n.15471+2T>C
XM_017000827.2:c.15456+2T>C	XP_016856316.2:n.15456+2T>C
XM_017000828.2:c.15432+2T>C	XP_016856317.2:n.15432+2T>C
XM_017000829.2:c.15384+2T>C	XP_016856318.2:n.15384+2T>C
XM_017000830.2:c.15333+2T>C	XP_016856319.2:n.15333+2T>C
NM_020765.3:c.15324+2T>C MANE Select	NP_065816.2:n.15324+2T>C