Canonical Allele Identifier: CA1346994371

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.14178523G= , CM000665.2:g.14178523G= GRCh38
NC_000003.11:g.14220023G= , CM000665.1:g.14220023G= GRCh37
NC_000003.10:g.14195027G= NCBI36
NG_011763.1:g.5150C= , LRG_472:g.5150C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000285021.12:c.46C= (XPC) MANE Select ENSP00000285021.8:p.Leu16=
ENST00000285021.11:c.46C= (XPC) ENSP00000285021.7:p.Leu16=
ENST00000306024.3:c.-338G= (LSM3) ENSP00000302160.3:n.-338G=
ENST00000476581.6:c.46C= (XPC) ENSP00000424548.1:p.Leu16=
ENST00000511155.1:c.46C= (XPC) ENSP00000423867.1:p.Leu16=
NM_004628.4:c.46C= , LRG_472t1:c.46C= (XPC) NP_004619.3:p.Leu16=
NR_027299.1:n.150C= (XPC)
XM_011534092.1:c.46C= (XPC) XP_011532394.1:p.Leu16=
XM_011534093.1:c.46C= (XPC) XP_011532395.1:p.Leu16=
NM_001354726.1:c.-410C= (XPC) NP_001341655.1:n.-410C=
NM_001354727.1:c.46C= (XPC) NP_001341656.1:p.Leu16=
NM_001354729.1:c.46C= (XPC) NP_001341658.1:p.Leu16=
NM_001354730.1:c.46C= (XPC) NP_001341659.1:p.Leu16=
NR_148950.1:n.150C= (XPC)
NR_148951.1:n.150C= (XPC)
XR_001740256.2:n.79C= (XPC)
XR_002959580.1:n.79C= (XPC)
XR_002959581.1:n.79C= (XPC)
NM_001354727.2:c.46C= (XPC) NP_001341656.1:p.Leu16=
NM_004628.5:c.46C= (XPC) MANE Select NP_004619.3:p.Leu16=
NR_148950.2:n.79C= (XPC)
NR_148951.2:n.79C= (XPC)
NM_001354726.2:c.-410C= (XPC) NP_001341655.1:n.-410C=
NM_001354729.2:c.46C= (XPC) NP_001341658.1:p.Leu16=
NM_001354730.2:c.46C= (XPC) NP_001341659.1:p.Leu16=