Canonical Allele Identifier: CA351541326

Gene: XPC

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.14158894T>C , CM000665.2:g.14158894T>C	GRCh38
NC_000003.11:g.14200394T>C , CM000665.1:g.14200394T>C	GRCh37
NC_000003.10:g.14175398T>C	NCBI36
NG_011763.1:g.24779A>G , LRG_472:g.24779A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_004628.5:c.991-2A>G MANE Select	NP_004619.3:n.991-2A>G
ENST00000285021.12:c.991-2A>G MANE Select	ENSP00000285021.8:n.991-2A>G
NM_001354726.1:c.412-2A>G	NP_001341655.1:n.412-2A>G
NM_001354726.2:c.412-2A>G	NP_001341655.1:n.412-2A>G
NM_001354727.1:c.991-2A>G	NP_001341656.1:n.991-2A>G
NM_001354727.2:c.991-2A>G	NP_001341656.1:n.991-2A>G
NM_001354729.1:c.973-2A>G	NP_001341658.1:n.973-2A>G
NM_001354729.2:c.973-2A>G	NP_001341658.1:n.973-2A>G
NM_001354730.1:c.991-2A>G	NP_001341659.1:n.991-2A>G
NM_001354730.2:c.991-2A>G	NP_001341659.1:n.991-2A>G
NM_004628.4:c.991-2A>G , LRG_472t1:c.991-2A>G	NP_004619.3:n.991-2A>G
NR_027299.1:n.971-2A>G
NR_148950.1:n.1095-2A>G
NR_148950.2:n.1024-2A>G
NR_148951.1:n.971-2A>G
NR_148951.2:n.900-2A>G
ENST00000285021.11:c.991-2A>G	ENSP00000285021.7:n.991-2A>G
ENST00000476581.6:c.*444-2A>G	ENSP00000424548.1:n.*444-2A>G
ENST00000477324.6:n.469-2A>G
XM_011534092.1:c.991-2A>G	XP_011532394.1:n.991-2A>G
XM_011534093.1:c.991-2A>G	XP_011532395.1:n.991-2A>G
XR_001740256.2:n.1024-2A>G
XR_002959580.1:n.1024-2A>G
XR_002959581.1:n.1024-2A>G