Canonical Allele Identifier: CA2561385020
Gene: ERCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.49524745_49524746insTTTGCACTGGGGCTGGAGGCGTGACTGGGGCTG , CM000672.2:g.49524745_49524746insTTTGCACTGGGGCTGGAGGCGTGACTGGGGCTG GRCh38
NC_000010.10:g.50732791_50732792insTTTGCACTGGGGCTGGAGGCGTGACTGGGGCTG , CM000672.1:g.50732791_50732792insTTTGCACTGGGGCTGGAGGCGTGACTGGGGCTG GRCh37
NC_000010.9:g.50402797_50402798insTTTGCACTGGGGCTGGAGGCGTGACTGGGGCTG NCBI36
NG_009442.1:g.19356_19357insCAGCCCCAGTCACGCCTCCAGCCCCAGTGCAAA , LRG_465:g.19356_19357insCAGCCCCAGTCACGCCTCCAGCCCCAGTGCAAA
NG_033155.1:g.4536_4537insCAGCCCCAGTCACGCCTCCAGCCCCAGTGCAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000355832.10:c.684_685insCAGCCCCAGTCACGCCTCCAGCCCCAGTGCAAA MANE Select ENSP00000348089.5:p.Leu228_Met229insGlnProGlnSerArgLeuGlnProG...
ENST00000447839.7:c.684_685insCAGCCCCAGTCACGCCTCCAGCCCCAGTGCAAA MANE Plus Clinical ENSP00000387966.2:p.Leu228_Met229insGlnProGlnSerArgLeuGlnProG...
ENST00000679596.1:c.*313_*314insCAGCCCCAGTCACGCCTCCAGCCCCAGTGCAAA ENSP00000504862.1:n.*313_*314insCAGCCCCAGTCACGCCTCCAGCCCCAGTG...
ENST00000679811.1:n.767_768insCAGCCCCAGTCACGCCTCCAGCCCCAGTGCAAA
ENST00000680107.1:c.652+3671_652+3672insCAGCCCCAGTCACGCCTCCAGCCCCAGTGCAAA ENSP00000505909.1:n.652+3671_652+3672insCAGCCCCAGTCACGCCTCCAG...
ENST00000680233.1:n.777_778insCAGCCCCAGTCACGCCTCCAGCCCCAGTGCAAA
ENST00000681632.1:n.762_763insCAGCCCCAGTCACGCCTCCAGCCCCAGTGCAAA
ENST00000681659.1:c.684_685insCAGCCCCAGTCACGCCTCCAGCCCCAGTGCAAA ENSP00000505631.1:p.Leu228_Met229insGlnProGlnSerArgLeuGlnProG...
ENST00000355832.9:c.684_685insCAGCCCCAGTCACGCCTCCAGCCCCAGTGCAAA ENSP00000348089.5:p.Leu228_Met229insGlnProGlnSerArgLeuGlnProG...
ENST00000447839.6:c.684_685insCAGCCCCAGTCACGCCTCCAGCCCCAGTGCAAA ENSP00000387966.2:p.Leu228_Met229insGlnProGlnSerArgLeuGlnProG...
ENST00000515869.1:c.684_685insCAGCCCCAGTCACGCCTCCAGCCCCAGTGCAAA ENSP00000423550.1:p.Leu228_Met229insGlnProGlnSerArgLeuGlnProG...
NM_000124.3:c.684_685insCAGCCCCAGTCACGCCTCCAGCCCCAGTGCAAA NP_000115.1:p.Leu228_Met229insGlnProGlnSerArgLeuGlnProGlnCysL...
NM_001277058.1:c.684_685insCAGCCCCAGTCACGCCTCCAGCCCCAGTGCAAA NP_001263987.1:p.Leu228_Met229insGlnProGlnSerArgLeuGlnProGlnC...
NM_001277059.1:c.684_685insCAGCCCCAGTCACGCCTCCAGCCCCAGTGCAAA NP_001263988.1:p.Leu228_Met229insGlnProGlnSerArgLeuGlnProGlnC...
NM_001346440.1:c.684_685insCAGCCCCAGTCACGCCTCCAGCCCCAGTGCAAA NP_001333369.1:p.Leu228_Met229insGlnProGlnSerArgLeuGlnProGlnC...
NM_000124.4:c.684_685insCAGCCCCAGTCACGCCTCCAGCCCCAGTGCAAA MANE Select NP_000115.1:p.Leu228_Met229insGlnProGlnSerArgLeuGlnProGlnCysL...
NM_001277058.2:c.684_685insCAGCCCCAGTCACGCCTCCAGCCCCAGTGCAAA MANE Plus Clinical NP_001263987.1:p.Leu228_Met229insGlnProGlnSerArgLeuGlnProGlnC...
NM_001277059.2:c.684_685insCAGCCCCAGTCACGCCTCCAGCCCCAGTGCAAA NP_001263988.1:p.Leu228_Met229insGlnProGlnSerArgLeuGlnProGlnC...
NM_001346440.2:c.684_685insCAGCCCCAGTCACGCCTCCAGCCCCAGTGCAAA NP_001333369.1:p.Leu228_Met229insGlnProGlnSerArgLeuGlnProGlnC...