Canonical Allele Identifier: CA1346950876

Gene: XPC

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.14148840G= , CM000665.2:g.14148840G=	GRCh38
NC_000003.11:g.14190340G= , CM000665.1:g.14190340G=	GRCh37
NC_000003.10:g.14165341G=	NCBI36
NG_011763.1:g.34833C= , LRG_472:g.34833C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285021.12:c.2224C= MANE Select	ENSP00000285021.8:p.Gln742=
ENST00000285021.11:c.2224C=	ENSP00000285021.7:p.Gln742=
ENST00000427795.2:n.89C=
ENST00000476581.6:c.*1677C=	ENSP00000424548.1:n.*1677C=
NM_004628.4:c.2224C= , LRG_472t1:c.2224C=	NP_004619.3:p.Gln742=
NR_027299.1:n.2204C=
XM_011534092.1:c.2224C=	XP_011532394.1:p.Gln742=
NM_001354726.1:c.1645C=	NP_001341655.1:p.Gln549=
NM_001354727.1:c.2218C=	NP_001341656.1:p.Gln740=
NM_001354729.1:c.2206C=	NP_001341658.1:p.Gln736=
NM_001354730.1:c.1978C=	NP_001341659.1:p.Gln660=
NR_148950.1:n.2167C=
NR_148951.1:n.2043C=
XR_001740256.2:n.2257C=
XR_002959580.1:n.2257C=
XR_002959581.1:n.3874C=
NM_001354727.2:c.2218C=	NP_001341656.1:p.Gln740=
NM_004628.5:c.2224C= MANE Select	NP_004619.3:p.Gln742=
NR_148950.2:n.2096C=
NR_148951.2:n.1972C=
NM_001354726.2:c.1645C=	NP_001341655.1:p.Gln549=
NM_001354729.2:c.2206C=	NP_001341658.1:p.Gln736=
NM_001354730.2:c.1978C=	NP_001341659.1:p.Gln660=