Canonical Allele Identifier: CA432813659

Gene: XPC

Linked Data

• MyVariant Identifiers: chr3:g.14190178A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.14148678A>C , CM000665.2:g.14148678A>C	GRCh38
NC_000003.11:g.14190178A>C , CM000665.1:g.14190178A>C	GRCh37
NC_000003.10:g.14165179A>C	NCBI36
NG_011763.1:g.34995T>G , LRG_472:g.34995T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285021.12:c.2304T>G MANE Select	ENSP00000285021.8:p.Pro768=
ENST00000285021.11:c.2304T>G	ENSP00000285021.7:p.Pro768=
ENST00000427795.2:n.169T>G
ENST00000476581.6:c.*1757T>G	ENSP00000424548.1:n.*1757T>G
NM_004628.4:c.2304T>G , LRG_472t1:c.2304T>G	NP_004619.3:p.Pro768=
NR_027299.1:n.2284T>G
XM_011534092.1:c.2304T>G	XP_011532394.1:p.Pro768=
NM_001354726.1:c.1725T>G	NP_001341655.1:p.Pro575=
NM_001354727.1:c.2298T>G	NP_001341656.1:p.Pro766=
NM_001354729.1:c.2286T>G	NP_001341658.1:p.Pro762=
NM_001354730.1:c.2058T>G	NP_001341659.1:p.Pro686=
NR_148950.1:n.2247T>G
NR_148951.1:n.2123T>G
XR_001740256.2:n.2337T>G
XR_002959580.1:n.2337T>G
XR_002959581.1:n.3954T>G
NM_001354727.2:c.2298T>G	NP_001341656.1:p.Pro766=
NM_004628.5:c.2304T>G MANE Select	NP_004619.3:p.Pro768=
NR_148950.2:n.2176T>G
NR_148951.2:n.2052T>G
NM_001354726.2:c.1725T>G	NP_001341655.1:p.Pro575=
NM_001354729.2:c.2286T>G	NP_001341658.1:p.Pro762=
NM_001354730.2:c.2058T>G	NP_001341659.1:p.Pro686=