Canonical Allele Identifier: CA1346950630

Gene: XPC

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.14148668C= , CM000665.2:g.14148668C=	GRCh38
NC_000003.11:g.14190168C= , CM000665.1:g.14190168C=	GRCh37
NC_000003.10:g.14165169C=	NCBI36
NG_011763.1:g.35005G= , LRG_472:g.35005G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285021.12:c.2314G= MANE Select	ENSP00000285021.8:p.Val772=
ENST00000285021.11:c.2314G=	ENSP00000285021.7:p.Val772=
ENST00000427795.2:n.179G=
ENST00000476581.6:c.*1767G=	ENSP00000424548.1:n.*1767G=
NM_004628.4:c.2314G= , LRG_472t1:c.2314G=	NP_004619.3:p.Val772=
NR_027299.1:n.2294G=
XM_011534092.1:c.2314G=	XP_011532394.1:p.Val772=
NM_001354726.1:c.1735G=	NP_001341655.1:p.Val579=
NM_001354727.1:c.2308G=	NP_001341656.1:p.Val770=
NM_001354729.1:c.2296G=	NP_001341658.1:p.Val766=
NM_001354730.1:c.2068G=	NP_001341659.1:p.Val690=
NR_148950.1:n.2257G=
NR_148951.1:n.2133G=
XR_001740256.2:n.2347G=
XR_002959580.1:n.2347G=
XR_002959581.1:n.3964G=
NM_001354727.2:c.2308G=	NP_001341656.1:p.Val770=
NM_004628.5:c.2314G= MANE Select	NP_004619.3:p.Val772=
NR_148950.2:n.2186G=
NR_148951.2:n.2062G=
NM_001354726.2:c.1735G=	NP_001341655.1:p.Val579=
NM_001354729.2:c.2296G=	NP_001341658.1:p.Val766=
NM_001354730.2:c.2068G=	NP_001341659.1:p.Val690=