Canonical Allele Identifier: CA338748100

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404485A>C (hg19) ; chr1:g.19077991A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19077991A>C , CM000663.2:g.19077991A>C	GRCh38
NC_000001.10:g.19404485A>C , CM000663.1:g.19404485A>C	GRCh37
NC_000001.9:g.19277072A>C	NCBI36
NG_027669.1:g.137262T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15309T>G MANE Select	ENSP00000364403.3:p.Ile5103Met
ENST00000375224.1:c.2430T>G	ENSP00000364372.1:p.Ile810Met
ENST00000375225.7:c.534T>G	ENSP00000364373.3:p.Ile178Met
ENST00000375254.7:c.15309T>G	ENSP00000364403.3:p.Ile5103Met
ENST00000459947.5:n.3316T>G
NM_020765.2:c.15309T>G	NP_065816.2:p.Ile5103Met
XM_011541108.1:c.15462T>G	XP_011539410.1:p.Ile5154Met
XM_011541109.1:c.15459T>G	XP_011539411.1:p.Ile5153Met
XM_011541110.1:c.15459T>G	XP_011539412.1:p.Ile5153Met
XM_011541111.1:c.15459T>G	XP_011539413.1:p.Ile5153Met
XM_011541112.1:c.15447T>G	XP_011539414.1:p.Ile5149Met
XM_011541113.1:c.15444T>G	XP_011539415.1:p.Ile5148Met
XM_011541114.1:c.15444T>G	XP_011539416.1:p.Ile5148Met
XM_011541115.1:c.15438T>G	XP_011539417.1:p.Ile5146Met
XM_011541116.1:c.15429T>G	XP_011539418.1:p.Ile5143Met
XM_011541117.1:c.15378T>G	XP_011539419.1:p.Ile5126Met
XM_011541118.1:c.15375T>G	XP_011539420.1:p.Ile5125Met
XM_011541119.1:c.15342T>G	XP_011539421.1:p.Ile5114Met
XM_011541120.1:c.15339T>G	XP_011539422.1:p.Ile5113Met
XM_011541121.1:c.15306T>G	XP_011539423.1:p.Ile5102Met
XM_011541108.3:c.15576T>G	XP_011539410.2:p.Ile5192Met
XM_011541109.3:c.15573T>G	XP_011539411.2:p.Ile5191Met
XM_011541110.3:c.15573T>G	XP_011539412.2:p.Ile5191Met
XM_011541111.3:c.15573T>G	XP_011539413.2:p.Ile5191Met
XM_011541112.3:c.15561T>G	XP_011539414.2:p.Ile5187Met
XM_011541113.3:c.15558T>G	XP_011539415.2:p.Ile5186Met
XM_011541114.3:c.15558T>G	XP_011539416.2:p.Ile5186Met
XM_011541115.3:c.15552T>G	XP_011539417.2:p.Ile5184Met
XM_011541116.3:c.15543T>G	XP_011539418.2:p.Ile5181Met
XM_011541117.3:c.15492T>G	XP_011539419.2:p.Ile5164Met
XM_011541118.3:c.15489T>G	XP_011539420.2:p.Ile5163Met
XM_011541119.3:c.15456T>G	XP_011539421.2:p.Ile5152Met
XM_011541120.3:c.15453T>G	XP_011539422.2:p.Ile5151Met
XM_011541121.3:c.15420T>G	XP_011539423.2:p.Ile5140Met
XM_017000822.2:c.15555T>G	XP_016856311.2:p.Ile5185Met
XM_017000823.2:c.15528T>G	XP_016856312.2:p.Ile5176Met
XM_017000824.2:c.15474T>G	XP_016856313.2:p.Ile5158Met
XM_017000825.2:c.15459T>G	XP_016856314.2:p.Ile5153Met
XM_017000826.2:c.15456T>G	XP_016856315.2:p.Ile5152Met
XM_017000827.2:c.15441T>G	XP_016856316.2:p.Ile5147Met
XM_017000828.2:c.15417T>G	XP_016856317.2:p.Ile5139Met
XM_017000829.2:c.15369T>G	XP_016856318.2:p.Ile5123Met
XM_017000830.2:c.15318T>G	XP_016856319.2:p.Ile5106Met
NM_020765.3:c.15309T>G MANE Select	NP_065816.2:p.Ile5103Met