Canonical Allele Identifier: CA406362940
Gene: ERCC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45352541T>C , CM000681.2:g.45352541T>C GRCh38
NC_000019.9:g.45855799T>C , CM000681.1:g.45855799T>C GRCh37
NC_000019.8:g.50547639T>C NCBI36
NG_007067.2:g.23047A>G , LRG_461:g.23047A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000391944.8:c.2011A>G ENSP00000375808.4:p.Lys671Glu
ENST00000682414.1:c.2011A>G ENSP00000507019.1:p.Lys671Glu
ENST00000682508.1:n.2040A>G
ENST00000684218.1:c.*1269A>G ENSP00000507804.1:n.*1269A>G
ENST00000684264.1:n.1567A>G
ENST00000684407.1:c.1888A>G ENSP00000507775.1:p.Lys630Glu
ENST00000684458.1:c.*497A>G ENSP00000508260.1:n.*497A>G
ENST00000684468.1:n.1723A>G
ENST00000391945.10:c.2011A>G MANE Select ENSP00000375809.4:p.Lys671Glu
ENST00000646507.1:n.2108A>G
ENST00000391941.6:c.1939A>G ENSP00000375805.2:p.Lys647Glu
ENST00000391942.6:n.1182A>G
ENST00000391944.7:c.1777A>G ENSP00000375808.3:p.Lys593Glu
ENST00000391945.8:c.2011A>G ENSP00000375809.3:p.Lys671Glu
ENST00000588652.5:n.2099A>G
NM_000400.3:c.2011A>G , LRG_461t1:c.2011A>G NP_000391.1:p.Lys671Glu
XM_011526611.1:c.1933A>G XP_011524913.1:p.Lys645Glu
XM_011526611.2:c.1933A>G XP_011524913.1:p.Lys645Glu
XM_017026467.1:c.1888A>G XP_016881956.1:p.Lys630Glu
XR_001753633.2:n.2058A>G
XR_001753634.2:n.1994A>G
NM_000400.4:c.2011A>G MANE Select NP_000391.1:p.Lys671Glu