Canonical Allele Identifier: CA1346950649

Gene: XPC

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.14148681C= , CM000665.2:g.14148681C=	GRCh38
NC_000003.11:g.14190181C= , CM000665.1:g.14190181C=	GRCh37
NC_000003.10:g.14165182C=	NCBI36
NG_011763.1:g.34992G= , LRG_472:g.34992G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285021.12:c.2301G= MANE Select	ENSP00000285021.8:p.Met767=
ENST00000285021.11:c.2301G=	ENSP00000285021.7:p.Met767=
ENST00000427795.2:n.166G=
ENST00000476581.6:c.*1754G=	ENSP00000424548.1:n.*1754G=
NM_004628.4:c.2301G= , LRG_472t1:c.2301G=	NP_004619.3:p.Met767=
NR_027299.1:n.2281G=
XM_011534092.1:c.2301G=	XP_011532394.1:p.Met767=
NM_001354726.1:c.1722G=	NP_001341655.1:p.Met574=
NM_001354727.1:c.2295G=	NP_001341656.1:p.Met765=
NM_001354729.1:c.2283G=	NP_001341658.1:p.Met761=
NM_001354730.1:c.2055G=	NP_001341659.1:p.Met685=
NR_148950.1:n.2244G=
NR_148951.1:n.2120G=
XR_001740256.2:n.2334G=
XR_002959580.1:n.2334G=
XR_002959581.1:n.3951G=
NM_001354727.2:c.2295G=	NP_001341656.1:p.Met765=
NM_004628.5:c.2301G= MANE Select	NP_004619.3:p.Met767=
NR_148950.2:n.2173G=
NR_148951.2:n.2049G=
NM_001354726.2:c.1722G=	NP_001341655.1:p.Met574=
NM_001354729.2:c.2283G=	NP_001341658.1:p.Met761=
NM_001354730.2:c.2055G=	NP_001341659.1:p.Met685=