Canonical Allele Identifier: CA416453002

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404479G>A (hg19)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15315C>T MANE Select	ENSP00000364403.3:p.Asn5105=
ENST00000375224.1:c.2436C>T	ENSP00000364372.1:p.Asn812=
ENST00000375225.7:c.540C>T	ENSP00000364373.3:p.Asn180=
ENST00000375254.7:c.15315C>T	ENSP00000364403.3:p.Asn5105=
ENST00000459947.5:n.3322C>T
NM_020765.2:c.15315C>T	NP_065816.2:p.Asn5105=
XM_011541108.1:c.15468C>T	XP_011539410.1:p.Asn5156=
XM_011541109.1:c.15465C>T	XP_011539411.1:p.Asn5155=
XM_011541110.1:c.15465C>T	XP_011539412.1:p.Asn5155=
XM_011541111.1:c.15465C>T	XP_011539413.1:p.Asn5155=
XM_011541112.1:c.15453C>T	XP_011539414.1:p.Asn5151=
XM_011541113.1:c.15450C>T	XP_011539415.1:p.Asn5150=
XM_011541114.1:c.15450C>T	XP_011539416.1:p.Asn5150=
XM_011541115.1:c.15444C>T	XP_011539417.1:p.Asn5148=
XM_011541116.1:c.15435C>T	XP_011539418.1:p.Asn5145=
XM_011541117.1:c.15384C>T	XP_011539419.1:p.Asn5128=
XM_011541118.1:c.15381C>T	XP_011539420.1:p.Asn5127=
XM_011541119.1:c.15348C>T	XP_011539421.1:p.Asn5116=
XM_011541120.1:c.15345C>T	XP_011539422.1:p.Asn5115=
XM_011541121.1:c.15312C>T	XP_011539423.1:p.Asn5104=
XM_011541108.3:c.15582C>T	XP_011539410.2:p.Asn5194=
XM_011541109.3:c.15579C>T	XP_011539411.2:p.Asn5193=
XM_011541110.3:c.15579C>T	XP_011539412.2:p.Asn5193=
XM_011541111.3:c.15579C>T	XP_011539413.2:p.Asn5193=
XM_011541112.3:c.15567C>T	XP_011539414.2:p.Asn5189=
XM_011541113.3:c.15564C>T	XP_011539415.2:p.Asn5188=
XM_011541114.3:c.15564C>T	XP_011539416.2:p.Asn5188=
XM_011541115.3:c.15558C>T	XP_011539417.2:p.Asn5186=
XM_011541116.3:c.15549C>T	XP_011539418.2:p.Asn5183=
XM_011541117.3:c.15498C>T	XP_011539419.2:p.Asn5166=
XM_011541118.3:c.15495C>T	XP_011539420.2:p.Asn5165=
XM_011541119.3:c.15462C>T	XP_011539421.2:p.Asn5154=
XM_011541120.3:c.15459C>T	XP_011539422.2:p.Asn5153=
XM_011541121.3:c.15426C>T	XP_011539423.2:p.Asn5142=
XM_017000822.2:c.15561C>T	XP_016856311.2:p.Asn5187=
XM_017000823.2:c.15534C>T	XP_016856312.2:p.Asn5178=
XM_017000824.2:c.15480C>T	XP_016856313.2:p.Asn5160=
XM_017000825.2:c.15465C>T	XP_016856314.2:p.Asn5155=
XM_017000826.2:c.15462C>T	XP_016856315.2:p.Asn5154=
XM_017000827.2:c.15447C>T	XP_016856316.2:p.Asn5149=
XM_017000828.2:c.15423C>T	XP_016856317.2:p.Asn5141=
XM_017000829.2:c.15375C>T	XP_016856318.2:p.Asn5125=
XM_017000830.2:c.15324C>T	XP_016856319.2:p.Asn5108=
NM_020765.3:c.15315C>T MANE Select	NP_065816.2:p.Asn5105=