Canonical Allele Identifier: CA2338388861
Gene: ERCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45352507T= , CM000681.2:g.45352507T= GRCh38
NC_000019.9:g.45855765T= , CM000681.1:g.45855765T= GRCh37
NC_000019.8:g.50547605T= NCBI36
NG_007067.2:g.23081A= , LRG_461:g.23081A=

Transcript Alleles

HGVS Amino-acid change
ENST00000391944.8:c.2045A= ENSP00000375808.4:p.Lys682=
ENST00000682414.1:c.2045A= ENSP00000507019.1:p.Lys682=
ENST00000682508.1:n.2074A=
ENST00000684218.1:c.*1303A= ENSP00000507804.1:n.*1303A=
ENST00000684264.1:n.1601A=
ENST00000684407.1:c.1922A= ENSP00000507775.1:p.Lys641=
ENST00000684458.1:c.*531A= ENSP00000508260.1:n.*531A=
ENST00000684468.1:n.1757A=
ENST00000391945.10:c.2045A= MANE Select ENSP00000375809.4:p.Lys682=
ENST00000646507.1:n.2142A=
ENST00000391941.6:c.1973A= ENSP00000375805.2:p.Lys658=
ENST00000391942.6:n.1216A=
ENST00000391944.7:c.1811A= ENSP00000375808.3:p.Lys604=
ENST00000391945.8:c.2045A= ENSP00000375809.3:p.Lys682=
ENST00000588652.5:n.2133A=
NM_000400.3:c.2045A= , LRG_461t1:c.2045A= NP_000391.1:p.Lys682=
XM_011526611.1:c.1967A= XP_011524913.1:p.Lys656=
XM_011526611.2:c.1967A= XP_011524913.1:p.Lys656=
XM_017026467.1:c.1922A= XP_016881956.1:p.Lys641=
XR_001753633.2:n.2092A=
XR_001753634.2:n.2028A=
NM_000400.4:c.2045A= MANE Select NP_000391.1:p.Lys682=