Canonical Allele Identifier: CA2338388709
Gene: ERCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45352263C= , CM000681.2:g.45352263C= GRCh38
NC_000019.9:g.45855521C= , CM000681.1:g.45855521C= GRCh37
NC_000019.8:g.50547361C= NCBI36
NG_007067.2:g.23325G= , LRG_461:g.23325G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000391944.8:c.2136G= ENSP00000375808.4:p.Glu712=
ENST00000682414.1:c.2136G= ENSP00000507019.1:p.Glu712=
ENST00000682508.1:n.2165G=
ENST00000684218.1:c.*1394G= ENSP00000507804.1:n.*1394G=
ENST00000684264.1:n.1692G=
ENST00000684407.1:c.2013G= ENSP00000507775.1:p.Glu671=
ENST00000684458.1:c.*622G= ENSP00000508260.1:n.*622G=
ENST00000684468.1:n.1848G=
ENST00000391945.10:c.2136G= MANE Select ENSP00000375809.4:p.Glu712=
ENST00000646507.1:n.2233G=
ENST00000391941.6:c.2064G= ENSP00000375805.2:p.Glu688=
ENST00000391942.6:n.1307G=
ENST00000391944.7:c.1902G= ENSP00000375808.3:p.Glu634=
ENST00000391945.8:c.2136G= ENSP00000375809.3:p.Glu712=
ENST00000588652.5:n.2224G=
NM_000400.3:c.2136G= , LRG_461t1:c.2136G= NP_000391.1:p.Glu712=
XM_011526611.1:c.2058G= XP_011524913.1:p.Glu686=
XM_011526611.2:c.2058G= XP_011524913.1:p.Glu686=
XM_017026467.1:c.2013G= XP_016881956.1:p.Glu671=
XR_001753633.2:n.2183G=
XR_001753634.2:n.2119G=
NM_000400.4:c.2136G= MANE Select NP_000391.1:p.Glu712=