Canonical Allele Identifier: CA432569842

Gene: XPC

Linked Data

• ClinVar Variation Id: 2000964
• ClinVar RCV Id: RCV002810775
• MyVariant Identifiers: chr3:g.14199682G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.14158182G>A , CM000665.2:g.14158182G>A	GRCh38
NC_000003.11:g.14199682G>A , CM000665.1:g.14199682G>A	GRCh37
NC_000003.10:g.14174684G>A	NCBI36
NG_011763.1:g.25491C>T , LRG_472:g.25491C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285021.12:c.1701C>T MANE Select	ENSP00000285021.8:p.Thr567=
ENST00000285021.11:c.1701C>T	ENSP00000285021.7:p.Thr567=
ENST00000476581.6:c.*1154C>T	ENSP00000424548.1:n.*1154C>T
NM_004628.4:c.1701C>T , LRG_472t1:c.1701C>T	NP_004619.3:p.Thr567=
NR_027299.1:n.1681C>T
XM_011534092.1:c.1701C>T	XP_011532394.1:p.Thr567=
XM_011534093.1:c.1701C>T	XP_011532395.1:p.Thr567=
NM_001354726.1:c.1122C>T	NP_001341655.1:p.Thr374=
NM_001354727.1:c.1701C>T	NP_001341656.1:p.Thr567=
NM_001354729.1:c.1683C>T	NP_001341658.1:p.Thr561=
NM_001354730.1:c.1626+75C>T	NP_001341659.1:n.1626+75C>T
NR_148950.1:n.1805C>T
NR_148951.1:n.1681C>T
XR_001740256.2:n.1734C>T
XR_002959580.1:n.1734C>T
XR_002959581.1:n.1734C>T
NM_001354727.2:c.1701C>T	NP_001341656.1:p.Thr567=
NM_004628.5:c.1701C>T MANE Select	NP_004619.3:p.Thr567=
NR_148950.2:n.1734C>T
NR_148951.2:n.1610C>T
NM_001354726.2:c.1122C>T	NP_001341655.1:p.Thr374=
NM_001354729.2:c.1683C>T	NP_001341658.1:p.Thr561=
NM_001354730.2:c.1626+75C>T	NP_001341659.1:n.1626+75C>T