Canonical Allele Identifier: CA338748078

Gene: UBR4

Linked Data

• gnomAD v4: 1-19077986-T-A
• MyVariant Identifiers: chr1:g.19404480T>A (hg19) ; chr1:g.19077986T>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15314A>T MANE Select	ENSP00000364403.3:p.Asn5105Ile
ENST00000375224.1:c.2435A>T	ENSP00000364372.1:p.Asn812Ile
ENST00000375225.7:c.539A>T	ENSP00000364373.3:p.Asn180Ile
ENST00000375254.7:c.15314A>T	ENSP00000364403.3:p.Asn5105Ile
ENST00000459947.5:n.3321A>T
NM_020765.2:c.15314A>T	NP_065816.2:p.Asn5105Ile
XM_011541108.1:c.15467A>T	XP_011539410.1:p.Asn5156Ile
XM_011541109.1:c.15464A>T	XP_011539411.1:p.Asn5155Ile
XM_011541110.1:c.15464A>T	XP_011539412.1:p.Asn5155Ile
XM_011541111.1:c.15464A>T	XP_011539413.1:p.Asn5155Ile
XM_011541112.1:c.15452A>T	XP_011539414.1:p.Asn5151Ile
XM_011541113.1:c.15449A>T	XP_011539415.1:p.Asn5150Ile
XM_011541114.1:c.15449A>T	XP_011539416.1:p.Asn5150Ile
XM_011541115.1:c.15443A>T	XP_011539417.1:p.Asn5148Ile
XM_011541116.1:c.15434A>T	XP_011539418.1:p.Asn5145Ile
XM_011541117.1:c.15383A>T	XP_011539419.1:p.Asn5128Ile
XM_011541118.1:c.15380A>T	XP_011539420.1:p.Asn5127Ile
XM_011541119.1:c.15347A>T	XP_011539421.1:p.Asn5116Ile
XM_011541120.1:c.15344A>T	XP_011539422.1:p.Asn5115Ile
XM_011541121.1:c.15311A>T	XP_011539423.1:p.Asn5104Ile
XM_011541108.3:c.15581A>T	XP_011539410.2:p.Asn5194Ile
XM_011541109.3:c.15578A>T	XP_011539411.2:p.Asn5193Ile
XM_011541110.3:c.15578A>T	XP_011539412.2:p.Asn5193Ile
XM_011541111.3:c.15578A>T	XP_011539413.2:p.Asn5193Ile
XM_011541112.3:c.15566A>T	XP_011539414.2:p.Asn5189Ile
XM_011541113.3:c.15563A>T	XP_011539415.2:p.Asn5188Ile
XM_011541114.3:c.15563A>T	XP_011539416.2:p.Asn5188Ile
XM_011541115.3:c.15557A>T	XP_011539417.2:p.Asn5186Ile
XM_011541116.3:c.15548A>T	XP_011539418.2:p.Asn5183Ile
XM_011541117.3:c.15497A>T	XP_011539419.2:p.Asn5166Ile
XM_011541118.3:c.15494A>T	XP_011539420.2:p.Asn5165Ile
XM_011541119.3:c.15461A>T	XP_011539421.2:p.Asn5154Ile
XM_011541120.3:c.15458A>T	XP_011539422.2:p.Asn5153Ile
XM_011541121.3:c.15425A>T	XP_011539423.2:p.Asn5142Ile
XM_017000822.2:c.15560A>T	XP_016856311.2:p.Asn5187Ile
XM_017000823.2:c.15533A>T	XP_016856312.2:p.Asn5178Ile
XM_017000824.2:c.15479A>T	XP_016856313.2:p.Asn5160Ile
XM_017000825.2:c.15464A>T	XP_016856314.2:p.Asn5155Ile
XM_017000826.2:c.15461A>T	XP_016856315.2:p.Asn5154Ile
XM_017000827.2:c.15446A>T	XP_016856316.2:p.Asn5149Ile
XM_017000828.2:c.15422A>T	XP_016856317.2:p.Asn5141Ile
XM_017000829.2:c.15374A>T	XP_016856318.2:p.Asn5125Ile
XM_017000830.2:c.15323A>T	XP_016856319.2:p.Asn5108Ile
NM_020765.3:c.15314A>T MANE Select	NP_065816.2:p.Asn5105Ile