Canonical Allele Identifier: CA2338391710
Gene: ERCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45357295A= , CM000681.2:g.45357295A= GRCh38
NC_000019.9:g.45860553A= , CM000681.1:g.45860553A= GRCh37
NC_000019.8:g.50552393A= NCBI36
NG_007067.2:g.18293T= , LRG_461:g.18293T=

Transcript Alleles

HGVS Amino-acid change
ENST00000391944.8:c.1454T= ENSP00000375808.4:p.Leu485=
ENST00000682414.1:c.1454T= ENSP00000507019.1:p.Leu485=
ENST00000682508.1:n.1483T=
ENST00000684218.1:c.*712T= ENSP00000507804.1:n.*712T=
ENST00000684264.1:n.1010T=
ENST00000684407.1:c.1331T= ENSP00000507775.1:p.Leu444=
ENST00000684458.1:c.*4T= ENSP00000508260.1:n.*4T=
ENST00000684468.1:n.1230T=
ENST00000391945.10:c.1454T= MANE Select ENSP00000375809.4:p.Leu485=
ENST00000587376.6:c.577T=
ENST00000646507.1:n.1551T=
ENST00000391941.6:c.1382T= ENSP00000375805.2:p.Leu461=
ENST00000391942.6:n.625T=
ENST00000391944.7:c.1220T= ENSP00000375808.3:p.Leu407=
ENST00000391945.8:c.1454T= ENSP00000375809.3:p.Leu485=
ENST00000587376.5:c.577T=
ENST00000588652.5:n.1542T=
NM_000400.3:c.1454T= , LRG_461t1:c.1454T= NP_000391.1:p.Leu485=
XM_011526611.1:c.1376T= XP_011524913.1:p.Leu459=
XR_935763.1:n.1501T=
XM_011526611.2:c.1376T= XP_011524913.1:p.Leu459=
XM_017026467.1:c.1331T= XP_016881956.1:p.Leu444=
XR_001753633.2:n.1501T=
XR_001753634.2:n.1501T=
NM_000400.4:c.1454T= MANE Select NP_000391.1:p.Leu485=