Canonical Allele Identifier: CA1346950595

Gene: XPC

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.14148645T= , CM000665.2:g.14148645T=	GRCh38
NC_000003.11:g.14190145T= , CM000665.1:g.14190145T=	GRCh37
NC_000003.10:g.14165146T=	NCBI36
NG_011763.1:g.35028A= , LRG_472:g.35028A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285021.12:c.2337A= MANE Select	ENSP00000285021.8:p.Leu779=
ENST00000285021.11:c.2337A=	ENSP00000285021.7:p.Leu779=
ENST00000427795.2:n.202A=
ENST00000476581.6:c.*1790A=	ENSP00000424548.1:n.*1790A=
NM_004628.4:c.2337A= , LRG_472t1:c.2337A=	NP_004619.3:p.Leu779=
NR_027299.1:n.2317A=
XM_011534092.1:c.2337A=	XP_011532394.1:p.Leu779=
NM_001354726.1:c.1758A=	NP_001341655.1:p.Leu586=
NM_001354727.1:c.2331A=	NP_001341656.1:p.Leu777=
NM_001354729.1:c.2319A=	NP_001341658.1:p.Leu773=
NM_001354730.1:c.2091A=	NP_001341659.1:p.Leu697=
NR_148950.1:n.2280A=
NR_148951.1:n.2156A=
XR_001740256.2:n.2370A=
XR_002959580.1:n.2370A=
XR_002959581.1:n.3987A=
NM_001354727.2:c.2331A=	NP_001341656.1:p.Leu777=
NM_004628.5:c.2337A= MANE Select	NP_004619.3:p.Leu779=
NR_148950.2:n.2209A=
NR_148951.2:n.2085A=
NM_001354726.2:c.1758A=	NP_001341655.1:p.Leu586=
NM_001354729.2:c.2319A=	NP_001341658.1:p.Leu773=
NM_001354730.2:c.2091A=	NP_001341659.1:p.Leu697=