Canonical Allele Identifier: CA1346950921

Gene: XPC

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.14148866A= , CM000665.2:g.14148866A=	GRCh38
NC_000003.11:g.14190366A= , CM000665.1:g.14190366A=	GRCh37
NC_000003.10:g.14165367A=	NCBI36
NG_011763.1:g.34807T= , LRG_472:g.34807T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285021.12:c.2198T= MANE Select	ENSP00000285021.8:p.Phe733=
ENST00000285021.11:c.2198T=	ENSP00000285021.7:p.Phe733=
ENST00000427795.2:n.63T=
ENST00000476581.6:c.*1651T=	ENSP00000424548.1:n.*1651T=
NM_004628.4:c.2198T= , LRG_472t1:c.2198T=	NP_004619.3:p.Phe733=
NR_027299.1:n.2178T=
XM_011534092.1:c.2198T=	XP_011532394.1:p.Phe733=
NM_001354726.1:c.1619T=	NP_001341655.1:p.Phe540=
NM_001354727.1:c.2192T=	NP_001341656.1:p.Phe731=
NM_001354729.1:c.2180T=	NP_001341658.1:p.Phe727=
NM_001354730.1:c.1952T=	NP_001341659.1:p.Phe651=
NR_148950.1:n.2141T=
NR_148951.1:n.2017T=
XR_001740256.2:n.2231T=
XR_002959580.1:n.2231T=
XR_002959581.1:n.3848T=
NM_001354727.2:c.2192T=	NP_001341656.1:p.Phe731=
NM_004628.5:c.2198T= MANE Select	NP_004619.3:p.Phe733=
NR_148950.2:n.2070T=
NR_148951.2:n.1946T=
NM_001354726.2:c.1619T=	NP_001341655.1:p.Phe540=
NM_001354729.2:c.2180T=	NP_001341658.1:p.Phe727=
NM_001354730.2:c.1952T=	NP_001341659.1:p.Phe651=