Canonical Allele Identifier: CA1346950647

Gene: XPC

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.14148679G= , CM000665.2:g.14148679G=	GRCh38
NC_000003.11:g.14190179G= , CM000665.1:g.14190179G=	GRCh37
NC_000003.10:g.14165180G=	NCBI36
NG_011763.1:g.34994C= , LRG_472:g.34994C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285021.12:c.2303C= MANE Select	ENSP00000285021.8:p.Pro768=
ENST00000285021.11:c.2303C=	ENSP00000285021.7:p.Pro768=
ENST00000427795.2:n.168C=
ENST00000476581.6:c.*1756C=	ENSP00000424548.1:n.*1756C=
NM_004628.4:c.2303C= , LRG_472t1:c.2303C=	NP_004619.3:p.Pro768=
NR_027299.1:n.2283C=
XM_011534092.1:c.2303C=	XP_011532394.1:p.Pro768=
NM_001354726.1:c.1724C=	NP_001341655.1:p.Pro575=
NM_001354727.1:c.2297C=	NP_001341656.1:p.Pro766=
NM_001354729.1:c.2285C=	NP_001341658.1:p.Pro762=
NM_001354730.1:c.2057C=	NP_001341659.1:p.Pro686=
NR_148950.1:n.2246C=
NR_148951.1:n.2122C=
XR_001740256.2:n.2336C=
XR_002959580.1:n.2336C=
XR_002959581.1:n.3953C=
NM_001354727.2:c.2297C=	NP_001341656.1:p.Pro766=
NM_004628.5:c.2303C= MANE Select	NP_004619.3:p.Pro768=
NR_148950.2:n.2175C=
NR_148951.2:n.2051C=
NM_001354726.2:c.1724C=	NP_001341655.1:p.Pro575=
NM_001354729.2:c.2285C=	NP_001341658.1:p.Pro762=
NM_001354730.2:c.2057C=	NP_001341659.1:p.Pro686=