Canonical Allele Identifier: CA351543417

Gene: XPC

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.14173064T>C , CM000665.2:g.14173064T>C	GRCh38
NC_000003.11:g.14214564T>C , CM000665.1:g.14214564T>C	GRCh37
NC_000003.10:g.14189568T>C	NCBI36
NG_011763.1:g.10609A>G , LRG_472:g.10609A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_004628.5:c.104-2A>G MANE Select	NP_004619.3:n.104-2A>G
ENST00000285021.12:c.104-2A>G MANE Select	ENSP00000285021.8:n.104-2A>G
NM_001354726.1:c.-352-2A>G	NP_001341655.1:n.-352-2A>G
NM_001354726.2:c.-352-2A>G	NP_001341655.1:n.-352-2A>G
NM_001354727.1:c.104-2A>G	NP_001341656.1:n.104-2A>G
NM_001354727.2:c.104-2A>G	NP_001341656.1:n.104-2A>G
NM_001354729.1:c.86-2A>G	NP_001341658.1:n.86-2A>G
NM_001354729.2:c.86-2A>G	NP_001341658.1:n.86-2A>G
NM_001354730.1:c.104-2A>G	NP_001341659.1:n.104-2A>G
NM_001354730.2:c.104-2A>G	NP_001341659.1:n.104-2A>G
NM_004628.4:c.104-2A>G , LRG_472t1:c.104-2A>G	NP_004619.3:n.104-2A>G
NR_027299.1:n.208-2A>G
NR_148950.1:n.208-2A>G
NR_148950.2:n.137-2A>G
NR_148951.1:n.208-2A>G
NR_148951.2:n.137-2A>G
ENST00000285021.11:c.104-2A>G	ENSP00000285021.7:n.104-2A>G
ENST00000476581.6:c.104-2A>G	ENSP00000424548.1:n.104-2A>G
ENST00000511155.1:c.86-2A>G	ENSP00000423867.1:n.86-2A>G
XM_011534092.1:c.104-2A>G	XP_011532394.1:n.104-2A>G
XM_011534093.1:c.104-2A>G	XP_011532395.1:n.104-2A>G
XR_001740256.2:n.137-2A>G
XR_002959580.1:n.137-2A>G
XR_002959581.1:n.137-2A>G