Canonical Allele Identifier: CA1346973950

Gene: XPC

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.14158882G= , CM000665.2:g.14158882G=	GRCh38
NC_000003.11:g.14200382G= , CM000665.1:g.14200382G=	GRCh37
NC_000003.10:g.14175386G=	NCBI36
NG_011763.1:g.24791C= , LRG_472:g.24791C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285021.12:c.1001C= MANE Select	ENSP00000285021.8:p.Pro334=
ENST00000285021.11:c.1001C=	ENSP00000285021.7:p.Pro334=
ENST00000476581.6:c.*454C=	ENSP00000424548.1:n.*454C=
ENST00000477324.6:n.479C=
NM_004628.4:c.1001C= , LRG_472t1:c.1001C=	NP_004619.3:p.Pro334=
NR_027299.1:n.981C=
XM_011534092.1:c.1001C=	XP_011532394.1:p.Pro334=
XM_011534093.1:c.1001C=	XP_011532395.1:p.Pro334=
NM_001354726.1:c.422C=	NP_001341655.1:p.Pro141=
NM_001354727.1:c.1001C=	NP_001341656.1:p.Pro334=
NM_001354729.1:c.983C=	NP_001341658.1:p.Pro328=
NM_001354730.1:c.1001C=	NP_001341659.1:p.Pro334=
NR_148950.1:n.1105C=
NR_148951.1:n.981C=
XR_001740256.2:n.1034C=
XR_002959580.1:n.1034C=
XR_002959581.1:n.1034C=
NM_001354727.2:c.1001C=	NP_001341656.1:p.Pro334=
NM_004628.5:c.1001C= MANE Select	NP_004619.3:p.Pro334=
NR_148950.2:n.1034C=
NR_148951.2:n.910C=
NM_001354726.2:c.422C=	NP_001341655.1:p.Pro141=
NM_001354729.2:c.983C=	NP_001341658.1:p.Pro328=
NM_001354730.2:c.1001C=	NP_001341659.1:p.Pro334=