Canonical Allele Identifier: CA1346947267

Gene: XPC

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.14145707_14145708delinsAG , CM000665.2:g.14145707_14145708delinsAG	GRCh38
NC_000003.11:g.14187207_14187208delinsAG , CM000665.1:g.14187207_14187208delinsAG	GRCh37
NC_000003.10:g.14162208_14162209delinsAG	NCBI36
NG_011763.1:g.37965_37966delinsCT , LRG_472:g.37965_37966delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000285021.12:c.*233_*234delinsCT MANE Select	ENSP00000285021.8:n.*233_*234delinsCT
ENST00000285021.11:c.*233_*234delinsCT	ENSP00000285021.7:n.*233_*234delinsCT
ENST00000601399.3:n.689+24_689+25delinsAG
ENST00000608606.1:c.598+24_598+25delinsAG
ENST00000626721.1:n.588+24_588+25delinsAG
NM_004628.4:c.*233_*234delinsCT , LRG_472t1:c.*233_*234delinsCT	NP_004619.3:n.*233_*234delinsCT
NR_027299.1:n.3036_3037delinsCT
NM_001354726.1:c.*233_*234delinsCT	NP_001341655.1:n.*233_*234delinsCT
NM_001354727.1:c.*233_*234delinsCT	NP_001341656.1:n.*233_*234delinsCT
NM_001354729.1:c.*233_*234delinsCT	NP_001341658.1:n.*233_*234delinsCT
NM_001354730.1:c.*233_*234delinsCT	NP_001341659.1:n.*233_*234delinsCT
NR_148950.1:n.2999_3000delinsCT
NR_148951.1:n.2875_2876delinsCT
XR_001740256.2:n.3363_3364delinsCT
XR_002959580.1:n.3438_3439delinsCT
XR_002959581.1:n.4706_4707delinsCT
NM_001354727.2:c.*233_*234delinsCT	NP_001341656.1:n.*233_*234delinsCT
NM_004628.5:c.*233_*234delinsCT MANE Select	NP_004619.3:n.*233_*234delinsCT
NR_148950.2:n.2928_2929delinsCT
NR_148951.2:n.2804_2805delinsCT
NM_001354726.2:c.*233_*234delinsCT	NP_001341655.1:n.*233_*234delinsCT
NM_001354729.2:c.*233_*234delinsCT	NP_001341658.1:n.*233_*234delinsCT
NM_001354730.2:c.*233_*234delinsCT	NP_001341659.1:n.*233_*234delinsCT