Canonical Allele Identifier: CA2338388757
Gene: ERCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45352342C= , CM000681.2:g.45352342C= GRCh38
NC_000019.9:g.45855600C= , CM000681.1:g.45855600C= GRCh37
NC_000019.8:g.50547440C= NCBI36
NG_007067.2:g.23246G= , LRG_461:g.23246G=

Transcript Alleles

HGVS Amino-acid change
ENST00000391944.8:c.2057G= ENSP00000375808.4:p.Arg686=
ENST00000682414.1:c.2057G= ENSP00000507019.1:p.Arg686=
ENST00000682508.1:n.2086G=
ENST00000684218.1:c.*1315G= ENSP00000507804.1:n.*1315G=
ENST00000684264.1:n.1613G=
ENST00000684407.1:c.1934G= ENSP00000507775.1:p.Arg645=
ENST00000684458.1:c.*543G= ENSP00000508260.1:n.*543G=
ENST00000684468.1:n.1769G=
ENST00000391945.10:c.2057G= MANE Select ENSP00000375809.4:p.Arg686=
ENST00000646507.1:n.2154G=
ENST00000391941.6:c.1985G= ENSP00000375805.2:p.Arg662=
ENST00000391942.6:n.1228G=
ENST00000391944.7:c.1823G= ENSP00000375808.3:p.Arg608=
ENST00000391945.8:c.2057G= ENSP00000375809.3:p.Arg686=
ENST00000588652.5:n.2145G=
NM_000400.3:c.2057G= , LRG_461t1:c.2057G= NP_000391.1:p.Arg686=
XM_011526611.1:c.1979G= XP_011524913.1:p.Arg660=
XM_011526611.2:c.1979G= XP_011524913.1:p.Arg660=
XM_017026467.1:c.1934G= XP_016881956.1:p.Arg645=
XR_001753633.2:n.2104G=
XR_001753634.2:n.2040G=
NM_000400.4:c.2057G= MANE Select NP_000391.1:p.Arg686=