Canonical Allele Identifier: CA351541499

Gene: XPC

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285021.12:c.905T>A MANE Select	ENSP00000285021.8:p.Phe302Tyr
ENST00000285021.11:c.905T>A	ENSP00000285021.7:p.Phe302Tyr
ENST00000476581.6:c.*358T>A	ENSP00000424548.1:n.*358T>A
ENST00000477324.6:n.383T>A
NM_004628.4:c.905T>A , LRG_472t1:c.905T>A	NP_004619.3:p.Phe302Tyr
NR_027299.1:n.885T>A
XM_011534092.1:c.905T>A	XP_011532394.1:p.Phe302Tyr
XM_011534093.1:c.905T>A	XP_011532395.1:p.Phe302Tyr
NM_001354726.1:c.326T>A	NP_001341655.1:p.Phe109Tyr
NM_001354727.1:c.905T>A	NP_001341656.1:p.Phe302Tyr
NM_001354729.1:c.887T>A	NP_001341658.1:p.Phe296Tyr
NM_001354730.1:c.905T>A	NP_001341659.1:p.Phe302Tyr
NR_148950.1:n.1009T>A
NR_148951.1:n.885T>A
XR_001740256.2:n.938T>A
XR_002959580.1:n.938T>A
XR_002959581.1:n.938T>A
NM_001354727.2:c.905T>A	NP_001341656.1:p.Phe302Tyr
NM_004628.5:c.905T>A MANE Select	NP_004619.3:p.Phe302Tyr
NR_148950.2:n.938T>A
NR_148951.2:n.814T>A
NM_001354726.2:c.326T>A	NP_001341655.1:p.Phe109Tyr
NM_001354729.2:c.887T>A	NP_001341658.1:p.Phe296Tyr
NM_001354730.2:c.905T>A	NP_001341659.1:p.Phe302Tyr