Canonical Allele Identifier: CA338748059

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404476C>G (hg19) ; chr1:g.19077982C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19077982C>G , CM000663.2:g.19077982C>G	GRCh38
NC_000001.10:g.19404476C>G , CM000663.1:g.19404476C>G	GRCh37
NC_000001.9:g.19277063C>G	NCBI36
NG_027669.1:g.137271G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15318G>C MANE Select	ENSP00000364403.3:p.Met5106Ile
ENST00000375224.1:c.2439G>C	ENSP00000364372.1:p.Met813Ile
ENST00000375225.7:c.543G>C	ENSP00000364373.3:p.Met181Ile
ENST00000375254.7:c.15318G>C	ENSP00000364403.3:p.Met5106Ile
ENST00000459947.5:n.3325G>C
NM_020765.2:c.15318G>C	NP_065816.2:p.Met5106Ile
XM_011541108.1:c.15471G>C	XP_011539410.1:p.Met5157Ile
XM_011541109.1:c.15468G>C	XP_011539411.1:p.Met5156Ile
XM_011541110.1:c.15468G>C	XP_011539412.1:p.Met5156Ile
XM_011541111.1:c.15468G>C	XP_011539413.1:p.Met5156Ile
XM_011541112.1:c.15456G>C	XP_011539414.1:p.Met5152Ile
XM_011541113.1:c.15453G>C	XP_011539415.1:p.Met5151Ile
XM_011541114.1:c.15453G>C	XP_011539416.1:p.Met5151Ile
XM_011541115.1:c.15447G>C	XP_011539417.1:p.Met5149Ile
XM_011541116.1:c.15438G>C	XP_011539418.1:p.Met5146Ile
XM_011541117.1:c.15387G>C	XP_011539419.1:p.Met5129Ile
XM_011541118.1:c.15384G>C	XP_011539420.1:p.Met5128Ile
XM_011541119.1:c.15351G>C	XP_011539421.1:p.Met5117Ile
XM_011541120.1:c.15348G>C	XP_011539422.1:p.Met5116Ile
XM_011541121.1:c.15315G>C	XP_011539423.1:p.Met5105Ile
XM_011541108.3:c.15585G>C	XP_011539410.2:p.Met5195Ile
XM_011541109.3:c.15582G>C	XP_011539411.2:p.Met5194Ile
XM_011541110.3:c.15582G>C	XP_011539412.2:p.Met5194Ile
XM_011541111.3:c.15582G>C	XP_011539413.2:p.Met5194Ile
XM_011541112.3:c.15570G>C	XP_011539414.2:p.Met5190Ile
XM_011541113.3:c.15567G>C	XP_011539415.2:p.Met5189Ile
XM_011541114.3:c.15567G>C	XP_011539416.2:p.Met5189Ile
XM_011541115.3:c.15561G>C	XP_011539417.2:p.Met5187Ile
XM_011541116.3:c.15552G>C	XP_011539418.2:p.Met5184Ile
XM_011541117.3:c.15501G>C	XP_011539419.2:p.Met5167Ile
XM_011541118.3:c.15498G>C	XP_011539420.2:p.Met5166Ile
XM_011541119.3:c.15465G>C	XP_011539421.2:p.Met5155Ile
XM_011541120.3:c.15462G>C	XP_011539422.2:p.Met5154Ile
XM_011541121.3:c.15429G>C	XP_011539423.2:p.Met5143Ile
XM_017000822.2:c.15564G>C	XP_016856311.2:p.Met5188Ile
XM_017000823.2:c.15537G>C	XP_016856312.2:p.Met5179Ile
XM_017000824.2:c.15483G>C	XP_016856313.2:p.Met5161Ile
XM_017000825.2:c.15468G>C	XP_016856314.2:p.Met5156Ile
XM_017000826.2:c.15465G>C	XP_016856315.2:p.Met5155Ile
XM_017000827.2:c.15450G>C	XP_016856316.2:p.Met5150Ile
XM_017000828.2:c.15426G>C	XP_016856317.2:p.Met5142Ile
XM_017000829.2:c.15378G>C	XP_016856318.2:p.Met5126Ile
XM_017000830.2:c.15327G>C	XP_016856319.2:p.Met5109Ile
NM_020765.3:c.15318G>C MANE Select	NP_065816.2:p.Met5106Ile