Canonical Allele Identifier: CA1346947608

Gene: XPC

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.14145949G= , CM000665.2:g.14145949G=	GRCh38
NC_000003.11:g.14187449G= , CM000665.1:g.14187449G=	GRCh37
NC_000003.10:g.14162450G=	NCBI36
NG_011763.1:g.37724C= , LRG_472:g.37724C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285021.12:c.2815C= MANE Select	ENSP00000285021.8:p.Gln939=
ENST00000285021.11:c.2815C=	ENSP00000285021.7:p.Gln939=
ENST00000476581.6:c.*2268C=	ENSP00000424548.1:n.*2268C=
ENST00000601399.3:n.689+266G=
ENST00000608606.1:c.598+266G=
ENST00000626721.1:n.588+266G=
NM_004628.4:c.2815C= , LRG_472t1:c.2815C=	NP_004619.3:p.Gln939=
NR_027299.1:n.2795C=
NM_001354726.1:c.2236C=	NP_001341655.1:p.Gln746=
NM_001354727.1:c.2809C=	NP_001341656.1:p.Gln937=
NM_001354729.1:c.2797C=	NP_001341658.1:p.Gln933=
NM_001354730.1:c.2569C=	NP_001341659.1:p.Gln857=
NR_148950.1:n.2758C=
NR_148951.1:n.2634C=
XR_001740256.2:n.3122C=
XR_002959580.1:n.3197C=
XR_002959581.1:n.4465C=
NM_001354727.2:c.2809C=	NP_001341656.1:p.Gln937=
NM_004628.5:c.2815C= MANE Select	NP_004619.3:p.Gln939=
NR_148950.2:n.2687C=
NR_148951.2:n.2563C=
NM_001354726.2:c.2236C=	NP_001341655.1:p.Gln746=
NM_001354729.2:c.2797C=	NP_001341658.1:p.Gln933=
NM_001354730.2:c.2569C=	NP_001341659.1:p.Gln857=