Canonical Allele Identifier: CA2266984

Gene: XPC

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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