Canonical Allele Identifier: CA1346961371

Gene: XPC

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.14158324G= , CM000665.2:g.14158324G=	GRCh38
NC_000003.11:g.14199824G= , CM000665.1:g.14199824G=	GRCh37
NC_000003.10:g.14174826G=	NCBI36
NG_011763.1:g.25349C= , LRG_472:g.25349C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285021.12:c.1559C= MANE Select	ENSP00000285021.8:p.Ala520=
ENST00000285021.11:c.1559C=	ENSP00000285021.7:p.Ala520=
ENST00000476581.6:c.*1012C=	ENSP00000424548.1:n.*1012C=
NM_004628.4:c.1559C= , LRG_472t1:c.1559C=	NP_004619.3:p.Ala520=
NR_027299.1:n.1539C=
XM_011534092.1:c.1559C=	XP_011532394.1:p.Ala520=
XM_011534093.1:c.1559C=	XP_011532395.1:p.Ala520=
NM_001354726.1:c.980C=	NP_001341655.1:p.Ala327=
NM_001354727.1:c.1559C=	NP_001341656.1:p.Ala520=
NM_001354729.1:c.1541C=	NP_001341658.1:p.Ala514=
NM_001354730.1:c.1559C=	NP_001341659.1:p.Ala520=
NR_148950.1:n.1663C=
NR_148951.1:n.1539C=
XR_001740256.2:n.1592C=
XR_002959580.1:n.1592C=
XR_002959581.1:n.1592C=
NM_001354727.2:c.1559C=	NP_001341656.1:p.Ala520=
NM_004628.5:c.1559C= MANE Select	NP_004619.3:p.Ala520=
NR_148950.2:n.1592C=
NR_148951.2:n.1468C=
NM_001354726.2:c.980C=	NP_001341655.1:p.Ala327=
NM_001354729.2:c.1541C=	NP_001341658.1:p.Ala514=
NM_001354730.2:c.1559C=	NP_001341659.1:p.Ala520=