Canonical Allele Identifier: CA1346988677

Gene: XPC

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.14166306G= , CM000665.2:g.14166306G=	GRCh38
NC_000003.11:g.14207806G= , CM000665.1:g.14207806G=	GRCh37
NC_000003.10:g.14182810G=	NCBI36
NG_011763.1:g.17367C= , LRG_472:g.17367C=

Transcript Alleles

HGVS	Amino-acid Change
NM_004628.5:c.622-721C= MANE Select	NP_004619.3:n.622-721C=
ENST00000285021.12:c.622-721C= MANE Select	ENSP00000285021.8:n.622-721C=
NM_001354726.1:c.43-721C=	NP_001341655.1:n.43-721C=
NM_001354726.2:c.43-721C=	NP_001341655.1:n.43-721C=
NM_001354727.1:c.622-721C=	NP_001341656.1:n.622-721C=
NM_001354727.2:c.622-721C=	NP_001341656.1:n.622-721C=
NM_001354729.1:c.604-721C=	NP_001341658.1:n.604-721C=
NM_001354729.2:c.604-721C=	NP_001341658.1:n.604-721C=
NM_001354730.1:c.622-721C=	NP_001341659.1:n.622-721C=
NM_001354730.2:c.622-721C=	NP_001341659.1:n.622-721C=
NM_004628.4:c.622-721C= , LRG_472t1:c.622-721C=	NP_004619.3:n.622-721C=
NR_027299.1:n.602-721C=
NR_148950.1:n.726-721C=
NR_148950.2:n.655-721C=
NR_148951.1:n.602-721C=
NR_148951.2:n.531-721C=
ENST00000285021.11:c.622-721C=	ENSP00000285021.7:n.622-721C=
ENST00000452172.1:n.387-721C=
ENST00000455144.6:n.233-721C=
ENST00000476581.6:c.*75-721C=	ENSP00000424548.1:n.*75-721C=
ENST00000477324.6:n.100-721C=
XM_011534092.1:c.622-721C=	XP_011532394.1:n.622-721C=
XM_011534093.1:c.622-721C=	XP_011532395.1:n.622-721C=
XR_001740256.2:n.655-721C=
XR_002959580.1:n.655-721C=
XR_002959581.1:n.655-721C=