Canonical Allele Identifier: CA351537645

Gene: XPC

Linked Data

• dbSNP Id: rs745660242
• gnomAD v3: 3-14148563-C-G
• gnomAD v4: 3-14148563-C-G
• MyVariant Identifiers: chr3:g.14190063C>G (hg19) ; chr3:g.14148563C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.14148563C>G , CM000665.2:g.14148563C>G	GRCh38
NC_000003.11:g.14190063C>G , CM000665.1:g.14190063C>G	GRCh37
NC_000003.10:g.14165064C>G	NCBI36
NG_011763.1:g.35110G>C , LRG_472:g.35110G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285021.12:c.2419G>C MANE Select	ENSP00000285021.8:p.Val807Leu
ENST00000285021.11:c.2419G>C	ENSP00000285021.7:p.Val807Leu
ENST00000427795.2:n.284G>C
ENST00000476581.6:c.*1872G>C	ENSP00000424548.1:n.*1872G>C
NM_004628.4:c.2419G>C , LRG_472t1:c.2419G>C	NP_004619.3:p.Val807Leu
NR_027299.1:n.2399G>C
XM_011534092.1:c.2419G>C	XP_011532394.1:p.Val807Leu
NM_001354726.1:c.1840G>C	NP_001341655.1:p.Val614Leu
NM_001354727.1:c.2413G>C	NP_001341656.1:p.Val805Leu
NM_001354729.1:c.2401G>C	NP_001341658.1:p.Val801Leu
NM_001354730.1:c.2173G>C	NP_001341659.1:p.Val725Leu
NR_148950.1:n.2362G>C
NR_148951.1:n.2238G>C
XR_001740256.2:n.2452G>C
XR_002959580.1:n.2452G>C
XR_002959581.1:n.4069G>C
NM_001354727.2:c.2413G>C	NP_001341656.1:p.Val805Leu
NM_004628.5:c.2419G>C MANE Select	NP_004619.3:p.Val807Leu
NR_148950.2:n.2291G>C
NR_148951.2:n.2167G>C
NM_001354726.2:c.1840G>C	NP_001341655.1:p.Val614Leu
NM_001354729.2:c.2401G>C	NP_001341658.1:p.Val801Leu
NM_001354730.2:c.2173G>C	NP_001341659.1:p.Val725Leu