Canonical Allele Identifier: CA351537888

Gene: XPC

Linked Data

• MyVariant Identifiers: chr3:g.14190180G>A (hg19) ; chr3:g.14148680G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.14148680G>A , CM000665.2:g.14148680G>A	GRCh38
NC_000003.11:g.14190180G>A , CM000665.1:g.14190180G>A	GRCh37
NC_000003.10:g.14165181G>A	NCBI36
NG_011763.1:g.34993C>T , LRG_472:g.34993C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285021.12:c.2302C>T MANE Select	ENSP00000285021.8:p.Pro768Ser
ENST00000285021.11:c.2302C>T	ENSP00000285021.7:p.Pro768Ser
ENST00000427795.2:n.167C>T
ENST00000476581.6:c.*1755C>T	ENSP00000424548.1:n.*1755C>T
NM_004628.4:c.2302C>T , LRG_472t1:c.2302C>T	NP_004619.3:p.Pro768Ser
NR_027299.1:n.2282C>T
XM_011534092.1:c.2302C>T	XP_011532394.1:p.Pro768Ser
NM_001354726.1:c.1723C>T	NP_001341655.1:p.Pro575Ser
NM_001354727.1:c.2296C>T	NP_001341656.1:p.Pro766Ser
NM_001354729.1:c.2284C>T	NP_001341658.1:p.Pro762Ser
NM_001354730.1:c.2056C>T	NP_001341659.1:p.Pro686Ser
NR_148950.1:n.2245C>T
NR_148951.1:n.2121C>T
XR_001740256.2:n.2335C>T
XR_002959580.1:n.2335C>T
XR_002959581.1:n.3952C>T
NM_001354727.2:c.2296C>T	NP_001341656.1:p.Pro766Ser
NM_004628.5:c.2302C>T MANE Select	NP_004619.3:p.Pro768Ser
NR_148950.2:n.2174C>T
NR_148951.2:n.2050C>T
NM_001354726.2:c.1723C>T	NP_001341655.1:p.Pro575Ser
NM_001354729.2:c.2284C>T	NP_001341658.1:p.Pro762Ser
NM_001354730.2:c.2056C>T	NP_001341659.1:p.Pro686Ser