Canonical Allele Identifier: CA899792194

Gene: XPC

Linked Data

• dbSNP Id: rs1216612289
• MyVariant Identifiers: chr3:g.14190240G>A (hg19) ; chr3:g.14148740G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.14148740G>A , CM000665.2:g.14148740G>A	GRCh38
NC_000003.11:g.14190240G>A , CM000665.1:g.14190240G>A	GRCh37
NC_000003.10:g.14165241G>A	NCBI36
NG_011763.1:g.34933C>T , LRG_472:g.34933C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285021.12:c.2251-9C>T MANE Select	ENSP00000285021.8:n.2251-9C>T
ENST00000285021.11:c.2251-9C>T	ENSP00000285021.7:n.2251-9C>T
ENST00000427795.2:n.116-9C>T
ENST00000476581.6:c.*1704-9C>T	ENSP00000424548.1:n.*1704-9C>T
NM_004628.4:c.2251-9C>T , LRG_472t1:c.2251-9C>T	NP_004619.3:n.2251-9C>T
NR_027299.1:n.2231-9C>T
XM_011534092.1:c.2251-9C>T	XP_011532394.1:n.2251-9C>T
NM_001354726.1:c.1672-9C>T	NP_001341655.1:n.1672-9C>T
NM_001354727.1:c.2245-9C>T	NP_001341656.1:n.2245-9C>T
NM_001354729.1:c.2233-9C>T	NP_001341658.1:n.2233-9C>T
NM_001354730.1:c.2005-9C>T	NP_001341659.1:n.2005-9C>T
NR_148950.1:n.2194-9C>T
NR_148951.1:n.2070-9C>T
XR_001740256.2:n.2284-9C>T
XR_002959580.1:n.2284-9C>T
XR_002959581.1:n.3901-9C>T
NM_001354727.2:c.2245-9C>T	NP_001341656.1:n.2245-9C>T
NM_004628.5:c.2251-9C>T MANE Select	NP_004619.3:n.2251-9C>T
NR_148950.2:n.2123-9C>T
NR_148951.2:n.1999-9C>T
NM_001354726.2:c.1672-9C>T	NP_001341655.1:n.1672-9C>T
NM_001354729.2:c.2233-9C>T	NP_001341658.1:n.2233-9C>T
NM_001354730.2:c.2005-9C>T	NP_001341659.1:n.2005-9C>T