Canonical Allele Identifier: CA1346961018

Gene: XPC

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.14158077C= , CM000665.2:g.14158077C=	GRCh38
NC_000003.11:g.14199577C= , CM000665.1:g.14199577C=	GRCh37
NC_000003.10:g.14174579C=	NCBI36
NG_011763.1:g.25596G= , LRG_472:g.25596G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285021.12:c.1806G= MANE Select	ENSP00000285021.8:p.Trp602=
ENST00000285021.11:c.1806G=	ENSP00000285021.7:p.Trp602=
ENST00000476581.6:c.*1259G=	ENSP00000424548.1:n.*1259G=
NM_004628.4:c.1806G= , LRG_472t1:c.1806G=	NP_004619.3:p.Trp602=
NR_027299.1:n.1786G=
XM_011534092.1:c.1806G=	XP_011532394.1:p.Trp602=
XM_011534093.1:c.1806G=	XP_011532395.1:p.Trp602=
NM_001354726.1:c.1227G=	NP_001341655.1:p.Trp409=
NM_001354727.1:c.1806G=	NP_001341656.1:p.Trp602=
NM_001354729.1:c.1788G=	NP_001341658.1:p.Trp596=
NM_001354730.1:c.1626+180G=	NP_001341659.1:n.1626+180G=
NR_148950.1:n.1910G=
NR_148951.1:n.1786G=
XR_001740256.2:n.1839G=
XR_002959580.1:n.1839G=
XR_002959581.1:n.1839G=
NM_001354727.2:c.1806G=	NP_001341656.1:p.Trp602=
NM_004628.5:c.1806G= MANE Select	NP_004619.3:p.Trp602=
NR_148950.2:n.1839G=
NR_148951.2:n.1715G=
NM_001354726.2:c.1227G=	NP_001341655.1:p.Trp409=
NM_001354729.2:c.1788G=	NP_001341658.1:p.Trp596=
NM_001354730.2:c.1626+180G=	NP_001341659.1:n.1626+180G=