Canonical Allele Identifier: CA2338388758
Gene: ERCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45352343G= , CM000681.2:g.45352343G= GRCh38
NC_000019.9:g.45855601G= , CM000681.1:g.45855601G= GRCh37
NC_000019.8:g.50547441G= NCBI36
NG_007067.2:g.23245C= , LRG_461:g.23245C=

Transcript Alleles

HGVS Amino-acid change
ENST00000391944.8:c.2056C= ENSP00000375808.4:p.Arg686=
ENST00000682414.1:c.2056C= ENSP00000507019.1:p.Arg686=
ENST00000682508.1:n.2085C=
ENST00000684218.1:c.*1314C= ENSP00000507804.1:n.*1314C=
ENST00000684264.1:n.1612C=
ENST00000684407.1:c.1933C= ENSP00000507775.1:p.Arg645=
ENST00000684458.1:c.*542C= ENSP00000508260.1:n.*542C=
ENST00000684468.1:n.1768C=
ENST00000391945.10:c.2056C= MANE Select ENSP00000375809.4:p.Arg686=
ENST00000646507.1:n.2153C=
ENST00000391941.6:c.1984C= ENSP00000375805.2:p.Arg662=
ENST00000391942.6:n.1227C=
ENST00000391944.7:c.1822C= ENSP00000375808.3:p.Arg608=
ENST00000391945.8:c.2056C= ENSP00000375809.3:p.Arg686=
ENST00000588652.5:n.2144C=
NM_000400.3:c.2056C= , LRG_461t1:c.2056C= NP_000391.1:p.Arg686=
XM_011526611.1:c.1978C= XP_011524913.1:p.Arg660=
XM_011526611.2:c.1978C= XP_011524913.1:p.Arg660=
XM_017026467.1:c.1933C= XP_016881956.1:p.Arg645=
XR_001753633.2:n.2103C=
XR_001753634.2:n.2039C=
NM_000400.4:c.2056C= MANE Select NP_000391.1:p.Arg686=