Canonical Allele Identifier: CA1346947491

Gene: XPC

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.14145857A= , CM000665.2:g.14145857A=	GRCh38
NC_000003.11:g.14187357A= , CM000665.1:g.14187357A=	GRCh37
NC_000003.10:g.14162358A=	NCBI36
NG_011763.1:g.37816T= , LRG_472:g.37816T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000285021.12:c.*84T= MANE Select	ENSP00000285021.8:n.*84T=
ENST00000285021.11:c.*84T=	ENSP00000285021.7:n.*84T=
ENST00000476581.6:c.*2360T=	ENSP00000424548.1:n.*2360T=
ENST00000601399.3:n.689+174A=
ENST00000608606.1:c.598+174A=
ENST00000626721.1:n.588+174A=
NM_004628.4:c.*84T= , LRG_472t1:c.*84T=	NP_004619.3:n.*84T=
NR_027299.1:n.2887T=
NM_001354726.1:c.*84T=	NP_001341655.1:n.*84T=
NM_001354727.1:c.*84T=	NP_001341656.1:n.*84T=
NM_001354729.1:c.*84T=	NP_001341658.1:n.*84T=
NM_001354730.1:c.*84T=	NP_001341659.1:n.*84T=
NR_148950.1:n.2850T=
NR_148951.1:n.2726T=
XR_001740256.2:n.3214T=
XR_002959580.1:n.3289T=
XR_002959581.1:n.4557T=
NM_001354727.2:c.*84T=	NP_001341656.1:n.*84T=
NM_004628.5:c.*84T= MANE Select	NP_004619.3:n.*84T=
NR_148950.2:n.2779T=
NR_148951.2:n.2655T=
NM_001354726.2:c.*84T=	NP_001341655.1:n.*84T=
NM_001354729.2:c.*84T=	NP_001341658.1:n.*84T=
NM_001354730.2:c.*84T=	NP_001341659.1:n.*84T=