Canonical Allele Identifier: CA351538983

Gene: XPC

Linked Data

• dbSNP Id: rs1180895832
• gnomAD v3: 3-14158066-G-C
• gnomAD v4: 3-14158066-G-C
• MyVariant Identifiers: chr3:g.14199566G>C (hg19) ; chr3:g.14158066G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.14158066G>C , CM000665.2:g.14158066G>C	GRCh38
NC_000003.11:g.14199566G>C , CM000665.1:g.14199566G>C	GRCh37
NC_000003.10:g.14174568G>C	NCBI36
NG_011763.1:g.25607C>G , LRG_472:g.25607C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285021.12:c.1817C>G MANE Select	ENSP00000285021.8:p.Thr606Ser
ENST00000285021.11:c.1817C>G	ENSP00000285021.7:p.Thr606Ser
ENST00000476581.6:c.*1270C>G	ENSP00000424548.1:n.*1270C>G
NM_004628.4:c.1817C>G , LRG_472t1:c.1817C>G	NP_004619.3:p.Thr606Ser
NR_027299.1:n.1797C>G
XM_011534092.1:c.1817C>G	XP_011532394.1:p.Thr606Ser
XM_011534093.1:c.1817C>G	XP_011532395.1:p.Thr606Ser
NM_001354726.1:c.1238C>G	NP_001341655.1:p.Thr413Ser
NM_001354727.1:c.1817C>G	NP_001341656.1:p.Thr606Ser
NM_001354729.1:c.1799C>G	NP_001341658.1:p.Thr600Ser
NM_001354730.1:c.1626+191C>G	NP_001341659.1:n.1626+191C>G
NR_148950.1:n.1921C>G
NR_148951.1:n.1797C>G
XR_001740256.2:n.1850C>G
XR_002959580.1:n.1850C>G
XR_002959581.1:n.1850C>G
NM_001354727.2:c.1817C>G	NP_001341656.1:p.Thr606Ser
NM_004628.5:c.1817C>G MANE Select	NP_004619.3:p.Thr606Ser
NR_148950.2:n.1850C>G
NR_148951.2:n.1726C>G
NM_001354726.2:c.1238C>G	NP_001341655.1:p.Thr413Ser
NM_001354729.2:c.1799C>G	NP_001341658.1:p.Thr600Ser
NM_001354730.2:c.1626+191C>G	NP_001341659.1:n.1626+191C>G