Canonical Allele Identifier: CA2338388904
Gene: ERCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45352573G= , CM000681.2:g.45352573G= GRCh38
NC_000019.9:g.45855831G= , CM000681.1:g.45855831G= GRCh37
NC_000019.8:g.50547671G= NCBI36
NG_007067.2:g.23015C= , LRG_461:g.23015C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000391944.8:c.1979C= ENSP00000375808.4:p.Ala660=
ENST00000682414.1:c.1979C= ENSP00000507019.1:p.Ala660=
ENST00000682508.1:n.2008C=
ENST00000684218.1:c.*1237C= ENSP00000507804.1:n.*1237C=
ENST00000684264.1:n.1535C=
ENST00000684407.1:c.1856C= ENSP00000507775.1:p.Ala619=
ENST00000684458.1:c.*465C= ENSP00000508260.1:n.*465C=
ENST00000684468.1:n.1691C=
ENST00000391945.10:c.1979C= MANE Select ENSP00000375809.4:p.Ala660=
ENST00000646507.1:n.2076C=
ENST00000391941.6:c.1907C= ENSP00000375805.2:p.Ala636=
ENST00000391942.6:n.1150C=
ENST00000391944.7:c.1745C= ENSP00000375808.3:p.Ala582=
ENST00000391945.8:c.1979C= ENSP00000375809.3:p.Ala660=
ENST00000588652.5:n.2067C=
NM_000400.3:c.1979C= , LRG_461t1:c.1979C= NP_000391.1:p.Ala660=
XM_011526611.1:c.1901C= XP_011524913.1:p.Ala634=
XM_011526611.2:c.1901C= XP_011524913.1:p.Ala634=
XM_017026467.1:c.1856C= XP_016881956.1:p.Ala619=
XR_001753633.2:n.2026C=
XR_001753634.2:n.1962C=
NM_000400.4:c.1979C= MANE Select NP_000391.1:p.Ala660=