Canonical Allele Identifier: CA2267376

Gene: XPC

Linked Data

• ClinVar Variation Id: 720863
• ClinVar RCV Id: RCV000894251 ; RCV001150643
• dbSNP Id: rs3731131
• ExAC: 3:14199649 G / T
• gnomAD v2: 3-14199649-G-T
• gnomAD v3: 3-14158149-G-T
• gnomAD v4: 3-14158149-G-T
• MyVariant Identifiers: chr3:g.14199649G>T (hg19) ; chr3:g.14158149G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.14158149G>T , CM000665.2:g.14158149G>T	GRCh38
NC_000003.11:g.14199649G>T , CM000665.1:g.14199649G>T	GRCh37
NC_000003.10:g.14174651G>T	NCBI36
NG_011763.1:g.25524C>A , LRG_472:g.25524C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285021.12:c.1734C>A MANE Select	ENSP00000285021.8:p.Val578=
ENST00000285021.11:c.1734C>A	ENSP00000285021.7:p.Val578=
ENST00000476581.6:c.*1187C>A	ENSP00000424548.1:n.*1187C>A
NM_004628.4:c.1734C>A , LRG_472t1:c.1734C>A	NP_004619.3:p.Val578=
NR_027299.1:n.1714C>A
XM_011534092.1:c.1734C>A	XP_011532394.1:p.Val578=
XM_011534093.1:c.1734C>A	XP_011532395.1:p.Val578=
NM_001354726.1:c.1155C>A	NP_001341655.1:p.Val385=
NM_001354727.1:c.1734C>A	NP_001341656.1:p.Val578=
NM_001354729.1:c.1716C>A	NP_001341658.1:p.Val572=
NM_001354730.1:c.1626+108C>A	NP_001341659.1:n.1626+108C>A
NR_148950.1:n.1838C>A
NR_148951.1:n.1714C>A
XR_001740256.2:n.1767C>A
XR_002959580.1:n.1767C>A
XR_002959581.1:n.1767C>A
NM_001354727.2:c.1734C>A	NP_001341656.1:p.Val578=
NM_004628.5:c.1734C>A MANE Select	NP_004619.3:p.Val578=
NR_148950.2:n.1767C>A
NR_148951.2:n.1643C>A
NM_001354726.2:c.1155C>A	NP_001341655.1:p.Val385=
NM_001354729.2:c.1716C>A	NP_001341658.1:p.Val572=
NM_001354730.2:c.1626+108C>A	NP_001341659.1:n.1626+108C>A