Canonical Allele Identifier: CA1346961203

Gene: XPC

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.14158178C= , CM000665.2:g.14158178C=	GRCh38
NC_000003.11:g.14199678C= , CM000665.1:g.14199678C=	GRCh37
NC_000003.10:g.14174680C=	NCBI36
NG_011763.1:g.25495G= , LRG_472:g.25495G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285021.12:c.1705G= MANE Select	ENSP00000285021.8:p.Val569=
ENST00000285021.11:c.1705G=	ENSP00000285021.7:p.Val569=
ENST00000476581.6:c.*1158G=	ENSP00000424548.1:n.*1158G=
NM_004628.4:c.1705G= , LRG_472t1:c.1705G=	NP_004619.3:p.Val569=
NR_027299.1:n.1685G=
XM_011534092.1:c.1705G=	XP_011532394.1:p.Val569=
XM_011534093.1:c.1705G=	XP_011532395.1:p.Val569=
NM_001354726.1:c.1126G=	NP_001341655.1:p.Val376=
NM_001354727.1:c.1705G=	NP_001341656.1:p.Val569=
NM_001354729.1:c.1687G=	NP_001341658.1:p.Val563=
NM_001354730.1:c.1626+79G=	NP_001341659.1:n.1626+79G=
NR_148950.1:n.1809G=
NR_148951.1:n.1685G=
XR_001740256.2:n.1738G=
XR_002959580.1:n.1738G=
XR_002959581.1:n.1738G=
NM_001354727.2:c.1705G=	NP_001341656.1:p.Val569=
NM_004628.5:c.1705G= MANE Select	NP_004619.3:p.Val569=
NR_148950.2:n.1738G=
NR_148951.2:n.1614G=
NM_001354726.2:c.1126G=	NP_001341655.1:p.Val376=
NM_001354729.2:c.1687G=	NP_001341658.1:p.Val563=
NM_001354730.2:c.1626+79G=	NP_001341659.1:n.1626+79G=