Canonical Allele Identifier: CA432813600

Gene: XPC

Linked Data

• gnomAD v4: 3-14148639-G-T
• MyVariant Identifiers: chr3:g.14190139G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.14148639G>T , CM000665.2:g.14148639G>T	GRCh38
NC_000003.11:g.14190139G>T , CM000665.1:g.14190139G>T	GRCh37
NC_000003.10:g.14165140G>T	NCBI36
NG_011763.1:g.35034C>A , LRG_472:g.35034C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000285021.12:c.2343C>A MANE Select	ENSP00000285021.8:p.Arg781=
ENST00000285021.11:c.2343C>A	ENSP00000285021.7:p.Arg781=
ENST00000427795.2:n.208C>A
ENST00000476581.6:c.*1796C>A	ENSP00000424548.1:n.*1796C>A
NM_004628.4:c.2343C>A , LRG_472t1:c.2343C>A	NP_004619.3:p.Arg781=
NR_027299.1:n.2323C>A
XM_011534092.1:c.2343C>A	XP_011532394.1:p.Arg781=
NM_001354726.1:c.1764C>A	NP_001341655.1:p.Arg588=
NM_001354727.1:c.2337C>A	NP_001341656.1:p.Arg779=
NM_001354729.1:c.2325C>A	NP_001341658.1:p.Arg775=
NM_001354730.1:c.2097C>A	NP_001341659.1:p.Arg699=
NR_148950.1:n.2286C>A
NR_148951.1:n.2162C>A
XR_001740256.2:n.2376C>A
XR_002959580.1:n.2376C>A
XR_002959581.1:n.3993C>A
NM_001354727.2:c.2337C>A	NP_001341656.1:p.Arg779=
NM_004628.5:c.2343C>A MANE Select	NP_004619.3:p.Arg781=
NR_148950.2:n.2215C>A
NR_148951.2:n.2091C>A
NM_001354726.2:c.1764C>A	NP_001341655.1:p.Arg588=
NM_001354729.2:c.2325C>A	NP_001341658.1:p.Arg775=
NM_001354730.2:c.2097C>A	NP_001341659.1:p.Arg699=