Canonical Allele Identifier: CA1346955497

Gene: XPC

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.14154182T= , CM000665.2:g.14154182T=	GRCh38
NC_000003.11:g.14195682T= , CM000665.1:g.14195682T=	GRCh37
NC_000003.10:g.14170683T=	NCBI36
NG_011763.1:g.29491A= , LRG_472:g.29491A=

Transcript Alleles

HGVS	Amino-acid Change
NM_004628.5:c.2034-1766A= MANE Select	NP_004619.3:n.2034-1766A=
ENST00000285021.12:c.2034-1766A= MANE Select	ENSP00000285021.8:n.2034-1766A=
NM_001354726.1:c.1455-1766A=	NP_001341655.1:n.1455-1766A=
NM_001354726.2:c.1455-1766A=	NP_001341655.1:n.1455-1766A=
NM_001354727.1:c.1873-149A=	NP_001341656.1:n.1873-149A=
NM_001354727.2:c.1873-149A=	NP_001341656.1:n.1873-149A=
NM_001354729.1:c.2016-1766A=	NP_001341658.1:n.2016-1766A=
NM_001354729.2:c.2016-1766A=	NP_001341658.1:n.2016-1766A=
NM_001354730.1:c.1788-1766A=	NP_001341659.1:n.1788-1766A=
NM_001354730.2:c.1788-1766A=	NP_001341659.1:n.1788-1766A=
NM_004628.4:c.2034-1766A= , LRG_472t1:c.2034-1766A=	NP_004619.3:n.2034-1766A=
NR_027299.1:n.2014-1766A=
NR_148950.1:n.1977-1766A=
NR_148950.2:n.1906-1766A=
NR_148951.1:n.1853-1766A=
NR_148951.2:n.1782-1766A=
ENST00000285021.11:c.2034-1766A=	ENSP00000285021.7:n.2034-1766A=
ENST00000476581.6:c.*1487-1766A=	ENSP00000424548.1:n.*1487-1766A=
XM_011534092.1:c.2034-1766A=	XP_011532394.1:n.2034-1766A=
XM_011534093.1:c.2034-149A=	XP_011532395.1:n.2034-149A=
XR_001740256.2:n.2067-1766A=
XR_002959580.1:n.2067-1766A=
XR_002959581.1:n.2067-149A=