Canonical Allele Identifier: CA432813623

Gene: XPC

Linked Data

• MyVariant Identifiers: chr3:g.14190151G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.14148651G>A , CM000665.2:g.14148651G>A	GRCh38
NC_000003.11:g.14190151G>A , CM000665.1:g.14190151G>A	GRCh37
NC_000003.10:g.14165152G>A	NCBI36
NG_011763.1:g.35022C>T , LRG_472:g.35022C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285021.12:c.2331C>T MANE Select	ENSP00000285021.8:p.Pro777=
ENST00000285021.11:c.2331C>T	ENSP00000285021.7:p.Pro777=
ENST00000427795.2:n.196C>T
ENST00000476581.6:c.*1784C>T	ENSP00000424548.1:n.*1784C>T
NM_004628.4:c.2331C>T , LRG_472t1:c.2331C>T	NP_004619.3:p.Pro777=
NR_027299.1:n.2311C>T
XM_011534092.1:c.2331C>T	XP_011532394.1:p.Pro777=
NM_001354726.1:c.1752C>T	NP_001341655.1:p.Pro584=
NM_001354727.1:c.2325C>T	NP_001341656.1:p.Pro775=
NM_001354729.1:c.2313C>T	NP_001341658.1:p.Pro771=
NM_001354730.1:c.2085C>T	NP_001341659.1:p.Pro695=
NR_148950.1:n.2274C>T
NR_148951.1:n.2150C>T
XR_001740256.2:n.2364C>T
XR_002959580.1:n.2364C>T
XR_002959581.1:n.3981C>T
NM_001354727.2:c.2325C>T	NP_001341656.1:p.Pro775=
NM_004628.5:c.2331C>T MANE Select	NP_004619.3:p.Pro777=
NR_148950.2:n.2203C>T
NR_148951.2:n.2079C>T
NM_001354726.2:c.1752C>T	NP_001341655.1:p.Pro584=
NM_001354729.2:c.2313C>T	NP_001341658.1:p.Pro771=
NM_001354730.2:c.2085C>T	NP_001341659.1:p.Pro695=