Canonical Allele Identifier: CA338748072

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404479G>C (hg19) ; chr1:g.19077985G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19077985G>C , CM000663.2:g.19077985G>C	GRCh38
NC_000001.10:g.19404479G>C , CM000663.1:g.19404479G>C	GRCh37
NC_000001.9:g.19277066G>C	NCBI36
NG_027669.1:g.137268C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15315C>G MANE Select	ENSP00000364403.3:p.Asn5105Lys
ENST00000375224.1:c.2436C>G	ENSP00000364372.1:p.Asn812Lys
ENST00000375225.7:c.540C>G	ENSP00000364373.3:p.Asn180Lys
ENST00000375254.7:c.15315C>G	ENSP00000364403.3:p.Asn5105Lys
ENST00000459947.5:n.3322C>G
NM_020765.2:c.15315C>G	NP_065816.2:p.Asn5105Lys
XM_011541108.1:c.15468C>G	XP_011539410.1:p.Asn5156Lys
XM_011541109.1:c.15465C>G	XP_011539411.1:p.Asn5155Lys
XM_011541110.1:c.15465C>G	XP_011539412.1:p.Asn5155Lys
XM_011541111.1:c.15465C>G	XP_011539413.1:p.Asn5155Lys
XM_011541112.1:c.15453C>G	XP_011539414.1:p.Asn5151Lys
XM_011541113.1:c.15450C>G	XP_011539415.1:p.Asn5150Lys
XM_011541114.1:c.15450C>G	XP_011539416.1:p.Asn5150Lys
XM_011541115.1:c.15444C>G	XP_011539417.1:p.Asn5148Lys
XM_011541116.1:c.15435C>G	XP_011539418.1:p.Asn5145Lys
XM_011541117.1:c.15384C>G	XP_011539419.1:p.Asn5128Lys
XM_011541118.1:c.15381C>G	XP_011539420.1:p.Asn5127Lys
XM_011541119.1:c.15348C>G	XP_011539421.1:p.Asn5116Lys
XM_011541120.1:c.15345C>G	XP_011539422.1:p.Asn5115Lys
XM_011541121.1:c.15312C>G	XP_011539423.1:p.Asn5104Lys
XM_011541108.3:c.15582C>G	XP_011539410.2:p.Asn5194Lys
XM_011541109.3:c.15579C>G	XP_011539411.2:p.Asn5193Lys
XM_011541110.3:c.15579C>G	XP_011539412.2:p.Asn5193Lys
XM_011541111.3:c.15579C>G	XP_011539413.2:p.Asn5193Lys
XM_011541112.3:c.15567C>G	XP_011539414.2:p.Asn5189Lys
XM_011541113.3:c.15564C>G	XP_011539415.2:p.Asn5188Lys
XM_011541114.3:c.15564C>G	XP_011539416.2:p.Asn5188Lys
XM_011541115.3:c.15558C>G	XP_011539417.2:p.Asn5186Lys
XM_011541116.3:c.15549C>G	XP_011539418.2:p.Asn5183Lys
XM_011541117.3:c.15498C>G	XP_011539419.2:p.Asn5166Lys
XM_011541118.3:c.15495C>G	XP_011539420.2:p.Asn5165Lys
XM_011541119.3:c.15462C>G	XP_011539421.2:p.Asn5154Lys
XM_011541120.3:c.15459C>G	XP_011539422.2:p.Asn5153Lys
XM_011541121.3:c.15426C>G	XP_011539423.2:p.Asn5142Lys
XM_017000822.2:c.15561C>G	XP_016856311.2:p.Asn5187Lys
XM_017000823.2:c.15534C>G	XP_016856312.2:p.Asn5178Lys
XM_017000824.2:c.15480C>G	XP_016856313.2:p.Asn5160Lys
XM_017000825.2:c.15465C>G	XP_016856314.2:p.Asn5155Lys
XM_017000826.2:c.15462C>G	XP_016856315.2:p.Asn5154Lys
XM_017000827.2:c.15447C>G	XP_016856316.2:p.Asn5149Lys
XM_017000828.2:c.15423C>G	XP_016856317.2:p.Asn5141Lys
XM_017000829.2:c.15375C>G	XP_016856318.2:p.Asn5125Lys
XM_017000830.2:c.15324C>G	XP_016856319.2:p.Asn5108Lys
NM_020765.3:c.15315C>G MANE Select	NP_065816.2:p.Asn5105Lys