Canonical Allele Identifier: CA1346953735

Gene: XPC

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.14152389C= , CM000665.2:g.14152389C=	GRCh38
NC_000003.11:g.14193889C= , CM000665.1:g.14193889C=	GRCh37
NC_000003.10:g.14168890C=	NCBI36
NG_011763.1:g.31284G= , LRG_472:g.31284G=

Transcript Alleles

HGVS	Amino-acid Change
NM_004628.5:c.2061G= MANE Select	NP_004619.3:p.Arg687=
ENST00000285021.12:c.2061G= MANE Select	ENSP00000285021.8:p.Arg687=
NM_001354726.1:c.1482G=	NP_001341655.1:p.Arg494=
NM_001354726.2:c.1482G=	NP_001341655.1:p.Arg494=
NM_001354727.1:c.2055G=	NP_001341656.1:p.Arg685=
NM_001354727.2:c.2055G=	NP_001341656.1:p.Arg685=
NM_001354729.1:c.2043G=	NP_001341658.1:p.Arg681=
NM_001354729.2:c.2043G=	NP_001341658.1:p.Arg681=
NM_001354730.1:c.1815G=	NP_001341659.1:p.Arg605=
NM_001354730.2:c.1815G=	NP_001341659.1:p.Arg605=
NM_004628.4:c.2061G= , LRG_472t1:c.2061G=	NP_004619.3:p.Arg687=
NR_027299.1:n.2041G=
NR_148950.1:n.2004G=
NR_148950.2:n.1933G=
NR_148951.1:n.1880G=
NR_148951.2:n.1809G=
ENST00000285021.11:c.2061G=	ENSP00000285021.7:p.Arg687=
ENST00000476581.6:c.*1514G=	ENSP00000424548.1:n.*1514G=
XM_011534092.1:c.2061G=	XP_011532394.1:p.Arg687=
XR_001740256.2:n.2094G=
XR_002959580.1:n.2094G=
XR_002959581.1:n.3711G=