Canonical Allele Identifier: CA2702103438

Gene: XPC

Linked Data

• dbSNP Id: rs2125003994

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.14145859G>A , CM000665.2:g.14145859G>A	GRCh38
NC_000003.11:g.14187359G>A , CM000665.1:g.14187359G>A	GRCh37
NC_000003.10:g.14162360G>A	NCBI36
NG_011763.1:g.37814C>T , LRG_472:g.37814C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000285021.12:c.*82C>T MANE Select	ENSP00000285021.8:n.*82C>T
ENST00000285021.11:c.*82C>T	ENSP00000285021.7:n.*82C>T
ENST00000476581.6:c.*2358C>T	ENSP00000424548.1:n.*2358C>T
ENST00000601399.3:n.689+176G>A
ENST00000608606.1:c.598+176G>A
ENST00000626721.1:n.588+176G>A
NM_004628.4:c.*82C>T , LRG_472t1:c.*82C>T	NP_004619.3:n.*82C>T
NR_027299.1:n.2885C>T
NM_001354726.1:c.*82C>T	NP_001341655.1:n.*82C>T
NM_001354727.1:c.*82C>T	NP_001341656.1:n.*82C>T
NM_001354729.1:c.*82C>T	NP_001341658.1:n.*82C>T
NM_001354730.1:c.*82C>T	NP_001341659.1:n.*82C>T
NR_148950.1:n.2848C>T
NR_148951.1:n.2724C>T
XR_001740256.2:n.3212C>T
XR_002959580.1:n.3287C>T
XR_002959581.1:n.4555C>T
NM_001354727.2:c.*82C>T	NP_001341656.1:n.*82C>T
NM_004628.5:c.*82C>T MANE Select	NP_004619.3:n.*82C>T
NR_148950.2:n.2777C>T
NR_148951.2:n.2653C>T
NM_001354726.2:c.*82C>T	NP_001341655.1:n.*82C>T
NM_001354729.2:c.*82C>T	NP_001341658.1:n.*82C>T
NM_001354730.2:c.*82C>T	NP_001341659.1:n.*82C>T