Canonical Allele Identifier: CA2338388760
Gene: ERCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45352345G= , CM000681.2:g.45352345G= GRCh38
NC_000019.9:g.45855603G= , CM000681.1:g.45855603G= GRCh37
NC_000019.8:g.50547443G= NCBI36
NG_007067.2:g.23243C= , LRG_461:g.23243C=

Transcript Alleles

HGVS Amino-acid change
ENST00000391944.8:c.2054C= ENSP00000375808.4:p.Ala685=
ENST00000682414.1:c.2054C= ENSP00000507019.1:p.Ala685=
ENST00000682508.1:n.2083C=
ENST00000684218.1:c.*1312C= ENSP00000507804.1:n.*1312C=
ENST00000684264.1:n.1610C=
ENST00000684407.1:c.1931C= ENSP00000507775.1:p.Ala644=
ENST00000684458.1:c.*540C= ENSP00000508260.1:n.*540C=
ENST00000684468.1:n.1766C=
ENST00000391945.10:c.2054C= MANE Select ENSP00000375809.4:p.Ala685=
ENST00000646507.1:n.2151C=
ENST00000391941.6:c.1982C= ENSP00000375805.2:p.Ala661=
ENST00000391942.6:n.1225C=
ENST00000391944.7:c.1820C= ENSP00000375808.3:p.Ala607=
ENST00000391945.8:c.2054C= ENSP00000375809.3:p.Ala685=
ENST00000588652.5:n.2142C=
NM_000400.3:c.2054C= , LRG_461t1:c.2054C= NP_000391.1:p.Ala685=
XM_011526611.1:c.1976C= XP_011524913.1:p.Ala659=
XM_011526611.2:c.1976C= XP_011524913.1:p.Ala659=
XM_017026467.1:c.1931C= XP_016881956.1:p.Ala644=
XR_001753633.2:n.2101C=
XR_001753634.2:n.2037C=
NM_000400.4:c.2054C= MANE Select NP_000391.1:p.Ala685=