Canonical Allele Identifier: CA338748076

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404480T>G (hg19) ; chr1:g.19077986T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19077986T>G , CM000663.2:g.19077986T>G	GRCh38
NC_000001.10:g.19404480T>G , CM000663.1:g.19404480T>G	GRCh37
NC_000001.9:g.19277067T>G	NCBI36
NG_027669.1:g.137267A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15314A>C MANE Select	ENSP00000364403.3:p.Asn5105Thr
ENST00000375224.1:c.2435A>C	ENSP00000364372.1:p.Asn812Thr
ENST00000375225.7:c.539A>C	ENSP00000364373.3:p.Asn180Thr
ENST00000375254.7:c.15314A>C	ENSP00000364403.3:p.Asn5105Thr
ENST00000459947.5:n.3321A>C
NM_020765.2:c.15314A>C	NP_065816.2:p.Asn5105Thr
XM_011541108.1:c.15467A>C	XP_011539410.1:p.Asn5156Thr
XM_011541109.1:c.15464A>C	XP_011539411.1:p.Asn5155Thr
XM_011541110.1:c.15464A>C	XP_011539412.1:p.Asn5155Thr
XM_011541111.1:c.15464A>C	XP_011539413.1:p.Asn5155Thr
XM_011541112.1:c.15452A>C	XP_011539414.1:p.Asn5151Thr
XM_011541113.1:c.15449A>C	XP_011539415.1:p.Asn5150Thr
XM_011541114.1:c.15449A>C	XP_011539416.1:p.Asn5150Thr
XM_011541115.1:c.15443A>C	XP_011539417.1:p.Asn5148Thr
XM_011541116.1:c.15434A>C	XP_011539418.1:p.Asn5145Thr
XM_011541117.1:c.15383A>C	XP_011539419.1:p.Asn5128Thr
XM_011541118.1:c.15380A>C	XP_011539420.1:p.Asn5127Thr
XM_011541119.1:c.15347A>C	XP_011539421.1:p.Asn5116Thr
XM_011541120.1:c.15344A>C	XP_011539422.1:p.Asn5115Thr
XM_011541121.1:c.15311A>C	XP_011539423.1:p.Asn5104Thr
XM_011541108.3:c.15581A>C	XP_011539410.2:p.Asn5194Thr
XM_011541109.3:c.15578A>C	XP_011539411.2:p.Asn5193Thr
XM_011541110.3:c.15578A>C	XP_011539412.2:p.Asn5193Thr
XM_011541111.3:c.15578A>C	XP_011539413.2:p.Asn5193Thr
XM_011541112.3:c.15566A>C	XP_011539414.2:p.Asn5189Thr
XM_011541113.3:c.15563A>C	XP_011539415.2:p.Asn5188Thr
XM_011541114.3:c.15563A>C	XP_011539416.2:p.Asn5188Thr
XM_011541115.3:c.15557A>C	XP_011539417.2:p.Asn5186Thr
XM_011541116.3:c.15548A>C	XP_011539418.2:p.Asn5183Thr
XM_011541117.3:c.15497A>C	XP_011539419.2:p.Asn5166Thr
XM_011541118.3:c.15494A>C	XP_011539420.2:p.Asn5165Thr
XM_011541119.3:c.15461A>C	XP_011539421.2:p.Asn5154Thr
XM_011541120.3:c.15458A>C	XP_011539422.2:p.Asn5153Thr
XM_011541121.3:c.15425A>C	XP_011539423.2:p.Asn5142Thr
XM_017000822.2:c.15560A>C	XP_016856311.2:p.Asn5187Thr
XM_017000823.2:c.15533A>C	XP_016856312.2:p.Asn5178Thr
XM_017000824.2:c.15479A>C	XP_016856313.2:p.Asn5160Thr
XM_017000825.2:c.15464A>C	XP_016856314.2:p.Asn5155Thr
XM_017000826.2:c.15461A>C	XP_016856315.2:p.Asn5154Thr
XM_017000827.2:c.15446A>C	XP_016856316.2:p.Asn5149Thr
XM_017000828.2:c.15422A>C	XP_016856317.2:p.Asn5141Thr
XM_017000829.2:c.15374A>C	XP_016856318.2:p.Asn5125Thr
XM_017000830.2:c.15323A>C	XP_016856319.2:p.Asn5108Thr
NM_020765.3:c.15314A>C MANE Select	NP_065816.2:p.Asn5105Thr