Canonical Allele Identifier: CA416452971

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404473A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19077979A>G , CM000663.2:g.19077979A>G	GRCh38
NC_000001.10:g.19404473A>G , CM000663.1:g.19404473A>G	GRCh37
NC_000001.9:g.19277060A>G	NCBI36
NG_027669.1:g.137274T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15321T>C MANE Select	ENSP00000364403.3:p.Phe5107=
ENST00000375224.1:c.2442T>C	ENSP00000364372.1:p.Phe814=
ENST00000375225.7:c.546T>C	ENSP00000364373.3:p.Phe182=
ENST00000375254.7:c.15321T>C	ENSP00000364403.3:p.Phe5107=
ENST00000459947.5:n.3328T>C
NM_020765.2:c.15321T>C	NP_065816.2:p.Phe5107=
XM_011541108.1:c.15474T>C	XP_011539410.1:p.Phe5158=
XM_011541109.1:c.15471T>C	XP_011539411.1:p.Phe5157=
XM_011541110.1:c.15471T>C	XP_011539412.1:p.Phe5157=
XM_011541111.1:c.15471T>C	XP_011539413.1:p.Phe5157=
XM_011541112.1:c.15459T>C	XP_011539414.1:p.Phe5153=
XM_011541113.1:c.15456T>C	XP_011539415.1:p.Phe5152=
XM_011541114.1:c.15456T>C	XP_011539416.1:p.Phe5152=
XM_011541115.1:c.15450T>C	XP_011539417.1:p.Phe5150=
XM_011541116.1:c.15441T>C	XP_011539418.1:p.Phe5147=
XM_011541117.1:c.15390T>C	XP_011539419.1:p.Phe5130=
XM_011541118.1:c.15387T>C	XP_011539420.1:p.Phe5129=
XM_011541119.1:c.15354T>C	XP_011539421.1:p.Phe5118=
XM_011541120.1:c.15351T>C	XP_011539422.1:p.Phe5117=
XM_011541121.1:c.15318T>C	XP_011539423.1:p.Phe5106=
XM_011541108.3:c.15588T>C	XP_011539410.2:p.Phe5196=
XM_011541109.3:c.15585T>C	XP_011539411.2:p.Phe5195=
XM_011541110.3:c.15585T>C	XP_011539412.2:p.Phe5195=
XM_011541111.3:c.15585T>C	XP_011539413.2:p.Phe5195=
XM_011541112.3:c.15573T>C	XP_011539414.2:p.Phe5191=
XM_011541113.3:c.15570T>C	XP_011539415.2:p.Phe5190=
XM_011541114.3:c.15570T>C	XP_011539416.2:p.Phe5190=
XM_011541115.3:c.15564T>C	XP_011539417.2:p.Phe5188=
XM_011541116.3:c.15555T>C	XP_011539418.2:p.Phe5185=
XM_011541117.3:c.15504T>C	XP_011539419.2:p.Phe5168=
XM_011541118.3:c.15501T>C	XP_011539420.2:p.Phe5167=
XM_011541119.3:c.15468T>C	XP_011539421.2:p.Phe5156=
XM_011541120.3:c.15465T>C	XP_011539422.2:p.Phe5155=
XM_011541121.3:c.15432T>C	XP_011539423.2:p.Phe5144=
XM_017000822.2:c.15567T>C	XP_016856311.2:p.Phe5189=
XM_017000823.2:c.15540T>C	XP_016856312.2:p.Phe5180=
XM_017000824.2:c.15486T>C	XP_016856313.2:p.Phe5162=
XM_017000825.2:c.15471T>C	XP_016856314.2:p.Phe5157=
XM_017000826.2:c.15468T>C	XP_016856315.2:p.Phe5156=
XM_017000827.2:c.15453T>C	XP_016856316.2:p.Phe5151=
XM_017000828.2:c.15429T>C	XP_016856317.2:p.Phe5143=
XM_017000829.2:c.15381T>C	XP_016856318.2:p.Phe5127=
XM_017000830.2:c.15330T>C	XP_016856319.2:p.Phe5110=
NM_020765.3:c.15321T>C MANE Select	NP_065816.2:p.Phe5107=