Canonical Allele Identifier: CA2838836136
Gene: ERCC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127292778_127292779insCAAGACTTCTTGGTGGCTATTGCAGAGCCAGTGTGCCG , CM000664.2:g.127292778_127292779insCAAGACTTCTTGGTGGCTATTGCAGAGCCAGTGTGCCG GRCh38
NC_000002.11:g.128050354_128050355insCAAGACTTCTTGGTGGCTATTGCAGAGCCAGTGTGCCG , CM000664.1:g.128050354_128050355insCAAGACTTCTTGGTGGCTATTGCAGAGCCAGTGTGCCG GRCh37
NC_000002.10:g.127766824_127766825insCAAGACTTCTTGGTGGCTATTGCAGAGCCAGTGTGCCG NCBI36
NG_007454.1:g.6398_6399insCGGCACACTGGCTCTGCAATAGCCACCAAGAAGTCTTG , LRG_462:g.6398_6399insCGGCACACTGGCTCTGCAATAGCCACCAAGAAGTCTTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000285398.7:c.302_303insCGGCACACTGGCTCTGCAATAGCCACCAAGAAGTCTTG MANE Select ENSP00000285398.2:p.Ala102GlyfsTer7
ENST00000642308.1:c.302_303insCGGCACACTGGCTCTGCAATAGCCACCAAGAAGTCTTG ENSP00000496684.1:p.Ala102GlyfsTer7
ENST00000644317.1:c.235-75_235-74insCGGCACACTGGCTCTGCAATAGCCACCAAGAAGTCTTG ENSP00000494012.1:n.235-75_235-74insCGGCACACTGGCTCTGCAATAGCCA...
ENST00000645233.1:c.302_303insCGGCACACTGGCTCTGCAATAGCCACCAAGAAGTCTTG ENSP00000494116.1:p.Ala102GlyfsTer7
ENST00000645467.1:c.302_303insCGGCACACTGGCTCTGCAATAGCCACCAAGAAGTCTTG ENSP00000494889.1:p.Ala102GlyfsTer7
ENST00000645736.1:c.158_159insCGGCACACTGGCTCTGCAATAGCCACCAAGAAGTCTTG ENSP00000494545.1:p.Ala54GlyfsTer7
ENST00000646654.1:c.302_303insCGGCACACTGGCTCTGCAATAGCCACCAAGAAGTCTTG ENSP00000494526.1:p.Ala102GlyfsTer7
ENST00000647169.1:c.302_303insCGGCACACTGGCTCTGCAATAGCCACCAAGAAGTCTTG ENSP00000495619.1:p.Ala102GlyfsTer7
ENST00000285398.6:c.302_303insCGGCACACTGGCTCTGCAATAGCCACCAAGAAGTCTTG ENSP00000285398.2:p.Ala102GlyfsTer7
ENST00000426778.5:c.*283_*284insCGGCACACTGGCTCTGCAATAGCCACCAAGAAGTCTTG ENSP00000415335.1:n.*283_*284insCGGCACACTGGCTCTGCAATAGCCACCAA...
ENST00000445889.5:c.*345_*346insCGGCACACTGGCTCTGCAATAGCCACCAAGAAGTCTTG ENSP00000390888.1:n.*345_*346insCGGCACACTGGCTCTGCAATAGCCACCAA...
ENST00000462306.5:n.291-75_291-74insCGGCACACTGGCTCTGCAATAGCCACCAAGAAGTCTTG
ENST00000490062.1:n.307-75_307-74insCGGCACACTGGCTCTGCAATAGCCACCAAGAAGTCTTG
ENST00000494464.5:n.261-75_261-74insCGGCACACTGGCTCTGCAATAGCCACCAAGAAGTCTTG
NM_000122.1:c.302_303insCGGCACACTGGCTCTGCAATAGCCACCAAGAAGTCTTG , LRG_462t1:c.302_303insCGGCACACTGGCTCTGCAATAGCCACCAAGAAGTCTTG NP_000113.1:p.Ala102GlyfsTer7
NM_001303416.1:c.110_111insCGGCACACTGGCTCTGCAATAGCCACCAAGAAGTCTTG NP_001290345.1:p.Ala38GlyfsTer7
NM_001303418.1:c.110_111insCGGCACACTGGCTCTGCAATAGCCACCAAGAAGTCTTG NP_001290347.1:p.Ala38GlyfsTer7
XM_011510794.1:c.302_303insCGGCACACTGGCTCTGCAATAGCCACCAAGAAGTCTTG XP_011509096.1:p.Ala102GlyfsTer7
XM_011510795.1:c.-80-75_-80-74insCGGCACACTGGCTCTGCAATAGCCACCAAGAAGTCTTG XP_011509097.1:n.-80-75_-80-74insCGGCACACTGGCTCTGCAATAGCCACCA...
XM_011510794.2:c.302_303insCGGCACACTGGCTCTGCAATAGCCACCAAGAAGTCTTG XP_011509096.1:p.Ala102GlyfsTer7
XM_017003583.1:c.-80-75_-80-74insCGGCACACTGGCTCTGCAATAGCCACCAAGAAGTCTTG XP_016859072.1:n.-80-75_-80-74insCGGCACACTGGCTCTGCAATAGCCACCA...
NM_000122.2:c.302_303insCGGCACACTGGCTCTGCAATAGCCACCAAGAAGTCTTG MANE Select NP_000113.1:p.Ala102GlyfsTer7
NM_001303416.2:c.110_111insCGGCACACTGGCTCTGCAATAGCCACCAAGAAGTCTTG NP_001290345.1:p.Ala38GlyfsTer7
NM_001303418.2:c.110_111insCGGCACACTGGCTCTGCAATAGCCACCAAGAAGTCTTG NP_001290347.1:p.Ala38GlyfsTer7