Canonical Allele Identifier: CA2338388910
Gene: ERCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45352580G= , CM000681.2:g.45352580G= GRCh38
NC_000019.9:g.45855838G= , CM000681.1:g.45855838G= GRCh37
NC_000019.8:g.50547678G= NCBI36
NG_007067.2:g.23008C= , LRG_461:g.23008C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000391944.8:c.1972C= ENSP00000375808.4:p.Arg658=
ENST00000682414.1:c.1972C= ENSP00000507019.1:p.Arg658=
ENST00000682508.1:n.2001C=
ENST00000684218.1:c.*1230C= ENSP00000507804.1:n.*1230C=
ENST00000684264.1:n.1528C=
ENST00000684407.1:c.1849C= ENSP00000507775.1:p.Arg617=
ENST00000684458.1:c.*458C= ENSP00000508260.1:n.*458C=
ENST00000684468.1:n.1684C=
ENST00000391945.10:c.1972C= MANE Select ENSP00000375809.4:p.Arg658=
ENST00000646507.1:n.2069C=
ENST00000391941.6:c.1900C= ENSP00000375805.2:p.Arg634=
ENST00000391942.6:n.1143C=
ENST00000391944.7:c.1738C= ENSP00000375808.3:p.Arg580=
ENST00000391945.8:c.1972C= ENSP00000375809.3:p.Arg658=
ENST00000588652.5:n.2060C=
NM_000400.3:c.1972C= , LRG_461t1:c.1972C= NP_000391.1:p.Arg658=
XM_011526611.1:c.1894C= XP_011524913.1:p.Arg632=
XM_011526611.2:c.1894C= XP_011524913.1:p.Arg632=
XM_017026467.1:c.1849C= XP_016881956.1:p.Arg617=
XR_001753633.2:n.2019C=
XR_001753634.2:n.1955C=
NM_000400.4:c.1972C= MANE Select NP_000391.1:p.Arg658=