Canonical Allele Identifier: CA2338388444
Gene: ERCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45351957C= , CM000681.2:g.45351957C= GRCh38
NC_000019.9:g.45855215C= , CM000681.1:g.45855215C= GRCh37
NC_000019.8:g.50547055C= NCBI36
NG_007067.2:g.23631G= , LRG_461:g.23631G=

Transcript Alleles

HGVS Amino-acid change
ENST00000391944.8:c.2442G= ENSP00000375808.4:p.Arg814=
ENST00000682414.1:c.2191-236G= ENSP00000507019.1:n.2191-236G=
ENST00000682508.1:n.2220-236G=
ENST00000684218.1:c.*1449-236G= ENSP00000507804.1:n.*1449-236G=
ENST00000684264.1:n.1747-236G=
ENST00000684407.1:c.2068-236G= ENSP00000507775.1:n.2068-236G=
ENST00000684458.1:c.*677-236G= ENSP00000508260.1:n.*677-236G=
ENST00000684468.1:n.1903-236G=
ENST00000391945.10:c.2191-236G= MANE Select ENSP00000375809.4:n.2191-236G=
ENST00000646507.1:n.2288-236G=
ENST00000391942.6:n.1362-236G=
ENST00000391944.7:c.1957-236G= ENSP00000375808.3:n.1957-236G=
ENST00000391945.8:c.2191-236G= ENSP00000375809.3:n.2191-236G=
ENST00000588652.5:n.2279-236G=
NM_000400.3:c.2191-236G= , LRG_461t1:c.2191-236G= NP_000391.1:n.2191-236G=
XM_011526611.1:c.2113-236G= XP_011524913.1:n.2113-236G=
XM_011526611.2:c.2113-236G= XP_011524913.1:n.2113-236G=
XM_017026467.1:c.2068-236G= XP_016881956.1:n.2068-236G=
XR_001753633.2:n.2238-236G=
XR_001753634.2:n.2174-236G=
NM_000400.4:c.2191-236G= MANE Select NP_000391.1:n.2191-236G=