Canonical Allele Identifier: CA351538629

Gene: XPC

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.14156399C>A , CM000665.2:g.14156399C>A	GRCh38
NC_000003.11:g.14197899C>A , CM000665.1:g.14197899C>A	GRCh37
NC_000003.10:g.14172901C>A	NCBI36
NG_011763.1:g.27274G>T , LRG_472:g.27274G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_004628.5:c.1969G>T MANE Select	NP_004619.3:p.Glu657Ter
ENST00000285021.12:c.1969G>T MANE Select	ENSP00000285021.8:p.Glu657Ter
NM_001354726.1:c.1390G>T	NP_001341655.1:p.Glu464Ter
NM_001354726.2:c.1390G>T	NP_001341655.1:p.Glu464Ter
NM_001354727.1:c.1872+1612G>T	NP_001341656.1:n.1872+1612G>T
NM_001354727.2:c.1872+1612G>T	NP_001341656.1:n.1872+1612G>T
NM_001354729.1:c.1951G>T	NP_001341658.1:p.Glu651Ter
NM_001354729.2:c.1951G>T	NP_001341658.1:p.Glu651Ter
NM_001354730.1:c.1723G>T	NP_001341659.1:p.Glu575Ter
NM_001354730.2:c.1723G>T	NP_001341659.1:p.Glu575Ter
NM_004628.4:c.1969G>T , LRG_472t1:c.1969G>T	NP_004619.3:p.Glu657Ter
NR_027299.1:n.1949G>T
NR_148950.1:n.1976+1612G>T
NR_148950.2:n.1905+1612G>T
NR_148951.1:n.1852+1612G>T
NR_148951.2:n.1781+1612G>T
ENST00000285021.11:c.1969G>T	ENSP00000285021.7:p.Glu657Ter
ENST00000476581.6:c.*1422G>T	ENSP00000424548.1:n.*1422G>T
XM_011534092.1:c.1969G>T	XP_011532394.1:p.Glu657Ter
XM_011534093.1:c.1969G>T	XP_011532395.1:p.Glu657Ter
XR_001740256.2:n.2002G>T
XR_002959580.1:n.2002G>T
XR_002959581.1:n.2002G>T