Canonical Allele Identifier: CA2338388611
Gene: ERCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45352135G= , CM000681.2:g.45352135G= GRCh38
NC_000019.9:g.45855393G= , CM000681.1:g.45855393G= GRCh37
NC_000019.8:g.50547233G= NCBI36
NG_007067.2:g.23453C= , LRG_461:g.23453C=

Transcript Alleles

HGVS Amino-acid change
ENST00000391945.10:c.2190+74C= MANE Select ENSP00000375809.4:p.=
ENST00000646507.1:n.2287+74C=
ENST00000391942.6:n.1361+74C=
ENST00000391944.7:c.1956+74C= ENSP00000375808.3:p.=
ENST00000391945.8:c.2190+74C= ENSP00000375809.3:p.=
ENST00000588652.5:n.2278+74C=
NM_000400.3:c.2190+74C= , LRG_461t1:c.2190+74C= NP_000391.1:p.=
XM_011526611.1:c.2112+74C= XP_011524913.1:p.=
XM_011526611.2:c.2112+74C= XP_011524913.1:p.=
XM_017026467.1:c.2067+74C= XP_016881956.1:p.=
XR_001753633.2:n.2237+74C=
XR_001753634.2:n.2173+74C=
NM_000400.4:c.2190+74C= MANE Select NP_000391.1:p.=