Canonical Allele Identifier: CA1346950943

Gene: XPC

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.14148879C= , CM000665.2:g.14148879C=	GRCh38
NC_000003.11:g.14190379C= , CM000665.1:g.14190379C=	GRCh37
NC_000003.10:g.14165380C=	NCBI36
NG_011763.1:g.34794G= , LRG_472:g.34794G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285021.12:c.2185G= MANE Select	ENSP00000285021.8:p.Asp729=
ENST00000285021.11:c.2185G=	ENSP00000285021.7:p.Asp729=
ENST00000427795.2:n.50G=
ENST00000476581.6:c.*1638G=	ENSP00000424548.1:n.*1638G=
NM_004628.4:c.2185G= , LRG_472t1:c.2185G=	NP_004619.3:p.Asp729=
NR_027299.1:n.2165G=
XM_011534092.1:c.2185G=	XP_011532394.1:p.Asp729=
NM_001354726.1:c.1606G=	NP_001341655.1:p.Asp536=
NM_001354727.1:c.2179G=	NP_001341656.1:p.Asp727=
NM_001354729.1:c.2167G=	NP_001341658.1:p.Asp723=
NM_001354730.1:c.1939G=	NP_001341659.1:p.Asp647=
NR_148950.1:n.2128G=
NR_148951.1:n.2004G=
XR_001740256.2:n.2218G=
XR_002959580.1:n.2218G=
XR_002959581.1:n.3835G=
NM_001354727.2:c.2179G=	NP_001341656.1:p.Asp727=
NM_004628.5:c.2185G= MANE Select	NP_004619.3:p.Asp729=
NR_148950.2:n.2057G=
NR_148951.2:n.1933G=
NM_001354726.2:c.1606G=	NP_001341655.1:p.Asp536=
NM_001354729.2:c.2167G=	NP_001341658.1:p.Asp723=
NM_001354730.2:c.1939G=	NP_001341659.1:p.Asp647=