Canonical Allele Identifier: CA1346961205

Gene: XPC

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.14158179A= , CM000665.2:g.14158179A=	GRCh38
NC_000003.11:g.14199679A= , CM000665.1:g.14199679A=	GRCh37
NC_000003.10:g.14174681A=	NCBI36
NG_011763.1:g.25494T= , LRG_472:g.25494T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285021.12:c.1704T= MANE Select	ENSP00000285021.8:p.Tyr568=
ENST00000285021.11:c.1704T=	ENSP00000285021.7:p.Tyr568=
ENST00000476581.6:c.*1157T=	ENSP00000424548.1:n.*1157T=
NM_004628.4:c.1704T= , LRG_472t1:c.1704T=	NP_004619.3:p.Tyr568=
NR_027299.1:n.1684T=
XM_011534092.1:c.1704T=	XP_011532394.1:p.Tyr568=
XM_011534093.1:c.1704T=	XP_011532395.1:p.Tyr568=
NM_001354726.1:c.1125T=	NP_001341655.1:p.Tyr375=
NM_001354727.1:c.1704T=	NP_001341656.1:p.Tyr568=
NM_001354729.1:c.1686T=	NP_001341658.1:p.Tyr562=
NM_001354730.1:c.1626+78T=	NP_001341659.1:n.1626+78T=
NR_148950.1:n.1808T=
NR_148951.1:n.1684T=
XR_001740256.2:n.1737T=
XR_002959580.1:n.1737T=
XR_002959581.1:n.1737T=
NM_001354727.2:c.1704T=	NP_001341656.1:p.Tyr568=
NM_004628.5:c.1704T= MANE Select	NP_004619.3:p.Tyr568=
NR_148950.2:n.1737T=
NR_148951.2:n.1613T=
NM_001354726.2:c.1125T=	NP_001341655.1:p.Tyr375=
NM_001354729.2:c.1686T=	NP_001341658.1:p.Tyr562=
NM_001354730.2:c.1626+78T=	NP_001341659.1:n.1626+78T=