Canonical Allele Identifier: CA351537767

Gene: XPC

Linked Data

• MyVariant Identifiers: chr3:g.14190119A>G (hg19) ; chr3:g.14148619A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.14148619A>G , CM000665.2:g.14148619A>G	GRCh38
NC_000003.11:g.14190119A>G , CM000665.1:g.14190119A>G	GRCh37
NC_000003.10:g.14165120A>G	NCBI36
NG_011763.1:g.35054T>C , LRG_472:g.35054T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285021.12:c.2363T>C MANE Select	ENSP00000285021.8:p.Ile788Thr
ENST00000285021.11:c.2363T>C	ENSP00000285021.7:p.Ile788Thr
ENST00000427795.2:n.228T>C
ENST00000476581.6:c.*1816T>C	ENSP00000424548.1:n.*1816T>C
NM_004628.4:c.2363T>C , LRG_472t1:c.2363T>C	NP_004619.3:p.Ile788Thr
NR_027299.1:n.2343T>C
XM_011534092.1:c.2363T>C	XP_011532394.1:p.Ile788Thr
NM_001354726.1:c.1784T>C	NP_001341655.1:p.Ile595Thr
NM_001354727.1:c.2357T>C	NP_001341656.1:p.Ile786Thr
NM_001354729.1:c.2345T>C	NP_001341658.1:p.Ile782Thr
NM_001354730.1:c.2117T>C	NP_001341659.1:p.Ile706Thr
NR_148950.1:n.2306T>C
NR_148951.1:n.2182T>C
XR_001740256.2:n.2396T>C
XR_002959580.1:n.2396T>C
XR_002959581.1:n.4013T>C
NM_001354727.2:c.2357T>C	NP_001341656.1:p.Ile786Thr
NM_004628.5:c.2363T>C MANE Select	NP_004619.3:p.Ile788Thr
NR_148950.2:n.2235T>C
NR_148951.2:n.2111T>C
NM_001354726.2:c.1784T>C	NP_001341655.1:p.Ile595Thr
NM_001354729.2:c.2345T>C	NP_001341658.1:p.Ile782Thr
NM_001354730.2:c.2117T>C	NP_001341659.1:p.Ile706Thr