Canonical Allele Identifier: CA1346950841

Gene: XPC

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.14148819C= , CM000665.2:g.14148819C=	GRCh38
NC_000003.11:g.14190319C= , CM000665.1:g.14190319C=	GRCh37
NC_000003.10:g.14165320C=	NCBI36
NG_011763.1:g.34854G= , LRG_472:g.34854G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285021.12:c.2245G= MANE Select	ENSP00000285021.8:p.Gly749=
ENST00000285021.11:c.2245G=	ENSP00000285021.7:p.Gly749=
ENST00000427795.2:n.110G=
ENST00000476581.6:c.*1698G=	ENSP00000424548.1:n.*1698G=
NM_004628.4:c.2245G= , LRG_472t1:c.2245G=	NP_004619.3:p.Gly749=
NR_027299.1:n.2225G=
XM_011534092.1:c.2245G=	XP_011532394.1:p.Gly749=
NM_001354726.1:c.1666G=	NP_001341655.1:p.Gly556=
NM_001354727.1:c.2239G=	NP_001341656.1:p.Gly747=
NM_001354729.1:c.2227G=	NP_001341658.1:p.Gly743=
NM_001354730.1:c.1999G=	NP_001341659.1:p.Gly667=
NR_148950.1:n.2188G=
NR_148951.1:n.2064G=
XR_001740256.2:n.2278G=
XR_002959580.1:n.2278G=
XR_002959581.1:n.3895G=
NM_001354727.2:c.2239G=	NP_001341656.1:p.Gly747=
NM_004628.5:c.2245G= MANE Select	NP_004619.3:p.Gly749=
NR_148950.2:n.2117G=
NR_148951.2:n.1993G=
NM_001354726.2:c.1666G=	NP_001341655.1:p.Gly556=
NM_001354729.2:c.2227G=	NP_001341658.1:p.Gly743=
NM_001354730.2:c.1999G=	NP_001341659.1:p.Gly667=