Canonical Allele Identifier: CA1346950547

Gene: XPC

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.14148609G= , CM000665.2:g.14148609G=	GRCh38
NC_000003.11:g.14190109G= , CM000665.1:g.14190109G=	GRCh37
NC_000003.10:g.14165110G=	NCBI36
NG_011763.1:g.35064C= , LRG_472:g.35064C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285021.12:c.2373C= MANE Select	ENSP00000285021.8:p.Val791=
ENST00000285021.11:c.2373C=	ENSP00000285021.7:p.Val791=
ENST00000427795.2:n.238C=
ENST00000476581.6:c.*1826C=	ENSP00000424548.1:n.*1826C=
NM_004628.4:c.2373C= , LRG_472t1:c.2373C=	NP_004619.3:p.Val791=
NR_027299.1:n.2353C=
XM_011534092.1:c.2373C=	XP_011532394.1:p.Val791=
NM_001354726.1:c.1794C=	NP_001341655.1:p.Val598=
NM_001354727.1:c.2367C=	NP_001341656.1:p.Val789=
NM_001354729.1:c.2355C=	NP_001341658.1:p.Val785=
NM_001354730.1:c.2127C=	NP_001341659.1:p.Val709=
NR_148950.1:n.2316C=
NR_148951.1:n.2192C=
XR_001740256.2:n.2406C=
XR_002959580.1:n.2406C=
XR_002959581.1:n.4023C=
NM_001354727.2:c.2367C=	NP_001341656.1:p.Val789=
NM_004628.5:c.2373C= MANE Select	NP_004619.3:p.Val791=
NR_148950.2:n.2245C=
NR_148951.2:n.2121C=
NM_001354726.2:c.1794C=	NP_001341655.1:p.Val598=
NM_001354729.2:c.2355C=	NP_001341658.1:p.Val785=
NM_001354730.2:c.2127C=	NP_001341659.1:p.Val709=