Canonical Allele Identifier: CA1346947464

Gene: XPC

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.14145845G= , CM000665.2:g.14145845G=	GRCh38
NC_000003.11:g.14187345G= , CM000665.1:g.14187345G=	GRCh37
NC_000003.10:g.14162346G=	NCBI36
NG_011763.1:g.37828C= , LRG_472:g.37828C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285021.12:c.*96C= MANE Select	ENSP00000285021.8:n.*96C=
ENST00000285021.11:c.*96C=	ENSP00000285021.7:n.*96C=
ENST00000476581.6:c.*2372C=	ENSP00000424548.1:n.*2372C=
ENST00000601399.3:n.689+162G=
ENST00000608606.1:c.598+162G=
ENST00000626721.1:n.588+162G=
NM_004628.4:c.*96C= , LRG_472t1:c.*96C=	NP_004619.3:n.*96C=
NR_027299.1:n.2899C=
NM_001354726.1:c.*96C=	NP_001341655.1:n.*96C=
NM_001354727.1:c.*96C=	NP_001341656.1:n.*96C=
NM_001354729.1:c.*96C=	NP_001341658.1:n.*96C=
NM_001354730.1:c.*96C=	NP_001341659.1:n.*96C=
NR_148950.1:n.2862C=
NR_148951.1:n.2738C=
XR_001740256.2:n.3226C=
XR_002959580.1:n.3301C=
XR_002959581.1:n.4569C=
NM_001354727.2:c.*96C=	NP_001341656.1:n.*96C=
NM_004628.5:c.*96C= MANE Select	NP_004619.3:n.*96C=
NR_148950.2:n.2791C=
NR_148951.2:n.2667C=
NM_001354726.2:c.*96C=	NP_001341655.1:n.*96C=
NM_001354729.2:c.*96C=	NP_001341658.1:n.*96C=
NM_001354730.2:c.*96C=	NP_001341659.1:n.*96C=