Canonical Allele Identifier: CA996294893
Gene: ERCC2 HGNC NCBI

Linked Data

dbSNP Id: rs1159650345

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45352133_45352139dup , CM000681.2:g.45352133_45352139dup GRCh38
NC_000019.9:g.45855391_45855397dup , CM000681.1:g.45855391_45855397dup GRCh37
NC_000019.8:g.50547231_50547237dup NCBI36
NG_007067.2:g.23457_23463dup , LRG_461:g.23457_23463dup

Transcript Alleles

HGVS Amino-acid change
ENST00000391944.8:c.2268_2274dup ENSP00000375808.4:p.Pro759SerfsTer?
ENST00000682414.1:c.2190+78_2190+84dup ENSP00000507019.1:n.2190+78_2190+84dup
ENST00000682508.1:n.2219+78_2219+84dup
ENST00000684218.1:c.*1448+78_*1448+84dup ENSP00000507804.1:n.*1448+78_*1448+84dup
ENST00000684264.1:n.1746+78_1746+84dup
ENST00000684407.1:c.2067+78_2067+84dup ENSP00000507775.1:n.2067+78_2067+84dup
ENST00000684458.1:c.*676+78_*676+84dup ENSP00000508260.1:n.*676+78_*676+84dup
ENST00000684468.1:n.1902+78_1902+84dup
ENST00000391945.10:c.2190+78_2190+84dup MANE Select ENSP00000375809.4:n.2190+78_2190+84dup
ENST00000646507.1:n.2287+78_2287+84dup
ENST00000391942.6:n.1361+78_1361+84dup
ENST00000391944.7:c.1956+78_1956+84dup ENSP00000375808.3:n.1956+78_1956+84dup
ENST00000391945.8:c.2190+78_2190+84dup ENSP00000375809.3:n.2190+78_2190+84dup
ENST00000588652.5:n.2278+78_2278+84dup
NM_000400.3:c.2190+78_2190+84dup , LRG_461t1:c.2190+78_2190+84dup NP_000391.1:n.2190+78_2190+84dup
XM_011526611.1:c.2112+78_2112+84dup XP_011524913.1:n.2112+78_2112+84dup
XM_011526611.2:c.2112+78_2112+84dup XP_011524913.1:n.2112+78_2112+84dup
XM_017026467.1:c.2067+78_2067+84dup XP_016881956.1:n.2067+78_2067+84dup
XR_001753633.2:n.2237+78_2237+84dup
XR_001753634.2:n.2173+78_2173+84dup
NM_000400.4:c.2190+78_2190+84dup MANE Select NP_000391.1:n.2190+78_2190+84dup