Canonical Allele Identifier: CA1346950964

Gene: XPC

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.14148895C= , CM000665.2:g.14148895C=	GRCh38
NC_000003.11:g.14190395C= , CM000665.1:g.14190395C=	GRCh37
NC_000003.10:g.14165396C=	NCBI36
NG_011763.1:g.34778G= , LRG_472:g.34778G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285021.12:c.2169G= MANE Select	ENSP00000285021.8:p.Gln723=
ENST00000285021.11:c.2169G=	ENSP00000285021.7:p.Gln723=
ENST00000427795.2:n.34G=
ENST00000476581.6:c.*1622G=	ENSP00000424548.1:n.*1622G=
NM_004628.4:c.2169G= , LRG_472t1:c.2169G=	NP_004619.3:p.Gln723=
NR_027299.1:n.2149G=
XM_011534092.1:c.2169G=	XP_011532394.1:p.Gln723=
NM_001354726.1:c.1590G=	NP_001341655.1:p.Gln530=
NM_001354727.1:c.2163G=	NP_001341656.1:p.Gln721=
NM_001354729.1:c.2151G=	NP_001341658.1:p.Gln717=
NM_001354730.1:c.1923G=	NP_001341659.1:p.Gln641=
NR_148950.1:n.2112G=
NR_148951.1:n.1988G=
XR_001740256.2:n.2202G=
XR_002959580.1:n.2202G=
XR_002959581.1:n.3819G=
NM_001354727.2:c.2163G=	NP_001341656.1:p.Gln721=
NM_004628.5:c.2169G= MANE Select	NP_004619.3:p.Gln723=
NR_148950.2:n.2041G=
NR_148951.2:n.1917G=
NM_001354726.2:c.1590G=	NP_001341655.1:p.Gln530=
NM_001354729.2:c.2151G=	NP_001341658.1:p.Gln717=
NM_001354730.2:c.1923G=	NP_001341659.1:p.Gln641=