Canonical Allele Identifier: CA2338391712
Gene: ERCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45357297C= , CM000681.2:g.45357297C= GRCh38
NC_000019.9:g.45860555C= , CM000681.1:g.45860555C= GRCh37
NC_000019.8:g.50552395C= NCBI36
NG_007067.2:g.18291G= , LRG_461:g.18291G=

Transcript Alleles

HGVS Amino-acid change
ENST00000391944.8:c.1452G= ENSP00000375808.4:p.Thr484=
ENST00000682414.1:c.1452G= ENSP00000507019.1:p.Thr484=
ENST00000682508.1:n.1481G=
ENST00000684218.1:c.*710G= ENSP00000507804.1:n.*710G=
ENST00000684264.1:n.1008G=
ENST00000684407.1:c.1329G= ENSP00000507775.1:p.Thr443=
ENST00000684458.1:c.*2G= ENSP00000508260.1:n.*2G=
ENST00000684468.1:n.1228G=
ENST00000391945.10:c.1452G= MANE Select ENSP00000375809.4:p.Thr484=
ENST00000587376.6:c.575G=
ENST00000646507.1:n.1549G=
ENST00000391941.6:c.1380G= ENSP00000375805.2:p.Thr460=
ENST00000391942.6:n.623G=
ENST00000391944.7:c.1218G= ENSP00000375808.3:p.Thr406=
ENST00000391945.8:c.1452G= ENSP00000375809.3:p.Thr484=
ENST00000587376.5:c.575G=
ENST00000588652.5:n.1540G=
NM_000400.3:c.1452G= , LRG_461t1:c.1452G= NP_000391.1:p.Thr484=
XM_011526611.1:c.1374G= XP_011524913.1:p.Thr458=
XR_935763.1:n.1499G=
XM_011526611.2:c.1374G= XP_011524913.1:p.Thr458=
XM_017026467.1:c.1329G= XP_016881956.1:p.Thr443=
XR_001753633.2:n.1499G=
XR_001753634.2:n.1499G=
NM_000400.4:c.1452G= MANE Select NP_000391.1:p.Thr484=