Canonical Allele Identifier: CA1346947375

Gene: XPC

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.14145785C= , CM000665.2:g.14145785C=	GRCh38
NC_000003.11:g.14187285C= , CM000665.1:g.14187285C=	GRCh37
NC_000003.10:g.14162286C=	NCBI36
NG_011763.1:g.37888G= , LRG_472:g.37888G=

Transcript Alleles

HGVS	Amino-acid Change
NM_004628.5:c.*156G= MANE Select	NP_004619.3:n.*156G=
ENST00000285021.12:c.*156G= MANE Select	ENSP00000285021.8:n.*156G=
NM_001354726.1:c.*156G=	NP_001341655.1:n.*156G=
NM_001354726.2:c.*156G=	NP_001341655.1:n.*156G=
NM_001354727.1:c.*156G=	NP_001341656.1:n.*156G=
NM_001354727.2:c.*156G=	NP_001341656.1:n.*156G=
NM_001354729.1:c.*156G=	NP_001341658.1:n.*156G=
NM_001354729.2:c.*156G=	NP_001341658.1:n.*156G=
NM_001354730.1:c.*156G=	NP_001341659.1:n.*156G=
NM_001354730.2:c.*156G=	NP_001341659.1:n.*156G=
NM_004628.4:c.*156G= , LRG_472t1:c.*156G=	NP_004619.3:n.*156G=
NR_027299.1:n.2959G=
NR_148950.1:n.2922G=
NR_148950.2:n.2851G=
NR_148951.1:n.2798G=
NR_148951.2:n.2727G=
ENST00000285021.11:c.*156G=	ENSP00000285021.7:n.*156G=
ENST00000476581.6:c.*2432G=	ENSP00000424548.1:n.*2432G=
ENST00000601399.3:n.689+102C=
ENST00000608606.1:c.598+102C=
ENST00000626721.1:n.588+102C=
XR_001740256.2:n.3286G=
XR_002959580.1:n.3361G=
XR_002959581.1:n.4629G=