Canonical Allele Identifier: CA1346951008

Gene: XPC

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.14148912G= , CM000665.2:g.14148912G=	GRCh38
NC_000003.11:g.14190412G= , CM000665.1:g.14190412G=	GRCh37
NC_000003.10:g.14165413G=	NCBI36
NG_011763.1:g.34761C= , LRG_472:g.34761C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285021.12:c.2152C= MANE Select	ENSP00000285021.8:p.Arg718=
ENST00000285021.11:c.2152C=	ENSP00000285021.7:p.Arg718=
ENST00000427795.2:n.17C=
ENST00000476581.6:c.*1605C=	ENSP00000424548.1:n.*1605C=
NM_004628.4:c.2152C= , LRG_472t1:c.2152C=	NP_004619.3:p.Arg718=
NR_027299.1:n.2132C=
XM_011534092.1:c.2152C=	XP_011532394.1:p.Arg718=
NM_001354726.1:c.1573C=	NP_001341655.1:p.Arg525=
NM_001354727.1:c.2146C=	NP_001341656.1:p.Arg716=
NM_001354729.1:c.2134C=	NP_001341658.1:p.Arg712=
NM_001354730.1:c.1906C=	NP_001341659.1:p.Arg636=
NR_148950.1:n.2095C=
NR_148951.1:n.1971C=
XR_001740256.2:n.2185C=
XR_002959580.1:n.2185C=
XR_002959581.1:n.3802C=
NM_001354727.2:c.2146C=	NP_001341656.1:p.Arg716=
NM_004628.5:c.2152C= MANE Select	NP_004619.3:p.Arg718=
NR_148950.2:n.2024C=
NR_148951.2:n.1900C=
NM_001354726.2:c.1573C=	NP_001341655.1:p.Arg525=
NM_001354729.2:c.2134C=	NP_001341658.1:p.Arg712=
NM_001354730.2:c.1906C=	NP_001341659.1:p.Arg636=