Canonical Allele Identifier: CA2267164

Gene: XPC

Linked Data

• ClinVar Variation Id: 735340
• ClinVar RCV Id: RCV000910875
• dbSNP Id: rs199828421
• ExAC: 3:14190064 G / A
• gnomAD v2: 3-14190064-G-A
• gnomAD v3: 3-14148564-G-A
• gnomAD v4: 3-14148564-G-A
• MyVariant Identifiers: chr3:g.14190064G>A (hg19) ; chr3:g.14148564G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.14148564G>A , CM000665.2:g.14148564G>A	GRCh38
NC_000003.11:g.14190064G>A , CM000665.1:g.14190064G>A	GRCh37
NC_000003.10:g.14165065G>A	NCBI36
NG_011763.1:g.35109C>T , LRG_472:g.35109C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285021.12:c.2418C>T MANE Select	ENSP00000285021.8:p.Pro806=
ENST00000285021.11:c.2418C>T	ENSP00000285021.7:p.Pro806=
ENST00000427795.2:n.283C>T
ENST00000476581.6:c.*1871C>T	ENSP00000424548.1:n.*1871C>T
NM_004628.4:c.2418C>T , LRG_472t1:c.2418C>T	NP_004619.3:p.Pro806=
NR_027299.1:n.2398C>T
XM_011534092.1:c.2418C>T	XP_011532394.1:p.Pro806=
NM_001354726.1:c.1839C>T	NP_001341655.1:p.Pro613=
NM_001354727.1:c.2412C>T	NP_001341656.1:p.Pro804=
NM_001354729.1:c.2400C>T	NP_001341658.1:p.Pro800=
NM_001354730.1:c.2172C>T	NP_001341659.1:p.Pro724=
NR_148950.1:n.2361C>T
NR_148951.1:n.2237C>T
XR_001740256.2:n.2451C>T
XR_002959580.1:n.2451C>T
XR_002959581.1:n.4068C>T
NM_001354727.2:c.2412C>T	NP_001341656.1:p.Pro804=
NM_004628.5:c.2418C>T MANE Select	NP_004619.3:p.Pro806=
NR_148950.2:n.2290C>T
NR_148951.2:n.2166C>T
NM_001354726.2:c.1839C>T	NP_001341655.1:p.Pro613=
NM_001354729.2:c.2400C>T	NP_001341658.1:p.Pro800=
NM_001354730.2:c.2172C>T	NP_001341659.1:p.Pro724=