Canonical Allele Identifier: CA1346950492

Gene: XPC

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.14148568T= , CM000665.2:g.14148568T=	GRCh38
NC_000003.11:g.14190068T= , CM000665.1:g.14190068T=	GRCh37
NC_000003.10:g.14165069T=	NCBI36
NG_011763.1:g.35105A= , LRG_472:g.35105A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285021.12:c.2414A= MANE Select	ENSP00000285021.8:p.His805=
ENST00000285021.11:c.2414A=	ENSP00000285021.7:p.His805=
ENST00000427795.2:n.279A=
ENST00000476581.6:c.*1867A=	ENSP00000424548.1:n.*1867A=
NM_004628.4:c.2414A= , LRG_472t1:c.2414A=	NP_004619.3:p.His805=
NR_027299.1:n.2394A=
XM_011534092.1:c.2414A=	XP_011532394.1:p.His805=
NM_001354726.1:c.1835A=	NP_001341655.1:p.His612=
NM_001354727.1:c.2408A=	NP_001341656.1:p.His803=
NM_001354729.1:c.2396A=	NP_001341658.1:p.His799=
NM_001354730.1:c.2168A=	NP_001341659.1:p.His723=
NR_148950.1:n.2357A=
NR_148951.1:n.2233A=
XR_001740256.2:n.2447A=
XR_002959580.1:n.2447A=
XR_002959581.1:n.4064A=
NM_001354727.2:c.2408A=	NP_001341656.1:p.His803=
NM_004628.5:c.2414A= MANE Select	NP_004619.3:p.His805=
NR_148950.2:n.2286A=
NR_148951.2:n.2162A=
NM_001354726.2:c.1835A=	NP_001341655.1:p.His612=
NM_001354729.2:c.2396A=	NP_001341658.1:p.His799=
NM_001354730.2:c.2168A=	NP_001341659.1:p.His723=