Canonical Allele Identifier: CA1346950559

Gene: XPC

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.14148623C= , CM000665.2:g.14148623C=	GRCh38
NC_000003.11:g.14190123C= , CM000665.1:g.14190123C=	GRCh37
NC_000003.10:g.14165124C=	NCBI36
NG_011763.1:g.35050G= , LRG_472:g.35050G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285021.12:c.2359G= MANE Select	ENSP00000285021.8:p.Asp787=
ENST00000285021.11:c.2359G=	ENSP00000285021.7:p.Asp787=
ENST00000427795.2:n.224G=
ENST00000476581.6:c.*1812G=	ENSP00000424548.1:n.*1812G=
NM_004628.4:c.2359G= , LRG_472t1:c.2359G=	NP_004619.3:p.Asp787=
NR_027299.1:n.2339G=
XM_011534092.1:c.2359G=	XP_011532394.1:p.Asp787=
NM_001354726.1:c.1780G=	NP_001341655.1:p.Asp594=
NM_001354727.1:c.2353G=	NP_001341656.1:p.Asp785=
NM_001354729.1:c.2341G=	NP_001341658.1:p.Asp781=
NM_001354730.1:c.2113G=	NP_001341659.1:p.Asp705=
NR_148950.1:n.2302G=
NR_148951.1:n.2178G=
XR_001740256.2:n.2392G=
XR_002959580.1:n.2392G=
XR_002959581.1:n.4009G=
NM_001354727.2:c.2353G=	NP_001341656.1:p.Asp785=
NM_004628.5:c.2359G= MANE Select	NP_004619.3:p.Asp787=
NR_148950.2:n.2231G=
NR_148951.2:n.2107G=
NM_001354726.2:c.1780G=	NP_001341655.1:p.Asp594=
NM_001354729.2:c.2341G=	NP_001341658.1:p.Asp781=
NM_001354730.2:c.2113G=	NP_001341659.1:p.Asp705=