Canonical Allele Identifier: CA1624127830

Gene: UBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.42594241C= , CM000668.2:g.42594241C=	GRCh38
NC_000006.11:g.42561979C= , CM000668.1:g.42561979C=	GRCh37
NC_000006.10:g.42669957C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372899.6:c.468C=	ENSP00000361990.1:p.Ala156=
ENST00000372901.2:c.468C= MANE Select	ENSP00000361992.1:p.Ala156=
ENST00000372899.5:c.468C=	ENSP00000361990.1:p.Ala156=
ENST00000372901.1:c.468C=	ENSP00000361992.1:p.Ala156=
ENST00000372903.6:c.468C=	ENSP00000361994.2:p.Ala156=
NM_001184801.1:c.468C=	NP_001171730.1:p.Ala156=
NM_015255.2:c.468C=	NP_056070.1:p.Ala156=
XM_005248965.3:c.468C=	XP_005249022.1:p.Ala156=
XM_011514438.1:c.282C=	XP_011512740.1:p.Ala94=
XM_011514442.1:c.468C=	XP_011512744.1:p.Ala156=
NM_001363705.1:c.468C=	NP_001350634.1:p.Ala156=
XM_005248966.3:c.-1638C=	XP_005249023.1:n.-1638C=
XM_011514438.2:c.549C=	XP_011512740.2:p.Ala183=
XM_017010594.1:c.549C=	XP_016866083.1:p.Ala183=
XM_017010595.1:c.549C=	XP_016866084.1:p.Ala183=
XM_017010596.1:c.468C=	XP_016866085.1:p.Ala156=
XM_017010597.1:c.549C=	XP_016866086.1:p.Ala183=
XR_001743284.2:n.967C=
XR_001743285.1:n.968C=
NM_001184801.2:c.468C=	NP_001171730.1:p.Ala156=
NM_001363705.2:c.468C= MANE Select	NP_001350634.1:p.Ala156=
NM_015255.3:c.468C=	NP_056070.1:p.Ala156=