Canonical Allele Identifier: CA1346974342

Gene: XPC

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.14159826A= , CM000665.2:g.14159826A=	GRCh38
NC_000003.11:g.14201326A= , CM000665.1:g.14201326A=	GRCh37
NC_000003.10:g.14176330A=	NCBI36
NG_011763.1:g.23847T= , LRG_472:g.23847T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285021.12:c.905T= MANE Select	ENSP00000285021.8:p.Phe302=
ENST00000285021.11:c.905T=	ENSP00000285021.7:p.Phe302=
ENST00000476581.6:c.*358T=	ENSP00000424548.1:n.*358T=
ENST00000477324.6:n.383T=
NM_004628.4:c.905T= , LRG_472t1:c.905T=	NP_004619.3:p.Phe302=
NR_027299.1:n.885T=
XM_011534092.1:c.905T=	XP_011532394.1:p.Phe302=
XM_011534093.1:c.905T=	XP_011532395.1:p.Phe302=
NM_001354726.1:c.326T=	NP_001341655.1:p.Phe109=
NM_001354727.1:c.905T=	NP_001341656.1:p.Phe302=
NM_001354729.1:c.887T=	NP_001341658.1:p.Phe296=
NM_001354730.1:c.905T=	NP_001341659.1:p.Phe302=
NR_148950.1:n.1009T=
NR_148951.1:n.885T=
XR_001740256.2:n.938T=
XR_002959580.1:n.938T=
XR_002959581.1:n.938T=
NM_001354727.2:c.905T=	NP_001341656.1:p.Phe302=
NM_004628.5:c.905T= MANE Select	NP_004619.3:p.Phe302=
NR_148950.2:n.938T=
NR_148951.2:n.814T=
NM_001354726.2:c.326T=	NP_001341655.1:p.Phe109=
NM_001354729.2:c.887T=	NP_001341658.1:p.Phe296=
NM_001354730.2:c.905T=	NP_001341659.1:p.Phe302=