Canonical Allele Identifier: CA2338391711
Gene: ERCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45357296G= , CM000681.2:g.45357296G= GRCh38
NC_000019.9:g.45860554G= , CM000681.1:g.45860554G= GRCh37
NC_000019.8:g.50552394G= NCBI36
NG_007067.2:g.18292C= , LRG_461:g.18292C=

Transcript Alleles

HGVS Amino-acid change
ENST00000391944.8:c.1453C= ENSP00000375808.4:p.Leu485=
ENST00000682414.1:c.1453C= ENSP00000507019.1:p.Leu485=
ENST00000682508.1:n.1482C=
ENST00000684218.1:c.*711C= ENSP00000507804.1:n.*711C=
ENST00000684264.1:n.1009C=
ENST00000684407.1:c.1330C= ENSP00000507775.1:p.Leu444=
ENST00000684458.1:c.*3C= ENSP00000508260.1:n.*3C=
ENST00000684468.1:n.1229C=
ENST00000391945.10:c.1453C= MANE Select ENSP00000375809.4:p.Leu485=
ENST00000587376.6:c.576C=
ENST00000646507.1:n.1550C=
ENST00000391941.6:c.1381C= ENSP00000375805.2:p.Leu461=
ENST00000391942.6:n.624C=
ENST00000391944.7:c.1219C= ENSP00000375808.3:p.Leu407=
ENST00000391945.8:c.1453C= ENSP00000375809.3:p.Leu485=
ENST00000587376.5:c.576C=
ENST00000588652.5:n.1541C=
NM_000400.3:c.1453C= , LRG_461t1:c.1453C= NP_000391.1:p.Leu485=
XM_011526611.1:c.1375C= XP_011524913.1:p.Leu459=
XR_935763.1:n.1500C=
XM_011526611.2:c.1375C= XP_011524913.1:p.Leu459=
XM_017026467.1:c.1330C= XP_016881956.1:p.Leu444=
XR_001753633.2:n.1500C=
XR_001753634.2:n.1500C=
NM_000400.4:c.1453C= MANE Select NP_000391.1:p.Leu485=