Canonical Allele Identifier: CA348391475
Community Standard Title: NM_000122.2(ERCC3):c.460C>T (p.Gln154Ter)
Gene: ERCC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127292621G>A , CM000664.2:g.127292621G>A GRCh38
NC_000002.11:g.128050197G>A , CM000664.1:g.128050197G>A GRCh37
NC_000002.10:g.127766667G>A NCBI36
NG_007454.1:g.6556C>T , LRG_462:g.6556C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000122.2:c.460C>T MANE Select NP_000113.1:p.Gln154Ter
ENST00000285398.7:c.460C>T MANE Select ENSP00000285398.2:p.Gln154Ter
NM_000122.1:c.460C>T , LRG_462t1:c.460C>T NP_000113.1:p.Gln154Ter
NM_001303416.1:c.268C>T NP_001290345.1:p.Gln90Ter
NM_001303416.2:c.268C>T NP_001290345.1:p.Gln90Ter
NM_001303418.1:c.268C>T NP_001290347.1:p.Gln90Ter
NM_001303418.2:c.268C>T NP_001290347.1:p.Gln90Ter
ENST00000285398.6:c.460C>T ENSP00000285398.2:p.Gln154Ter
ENST00000426778.5:c.*441C>T ENSP00000415335.1:n.*441C>T
ENST00000445889.5:c.*503C>T ENSP00000390888.1:n.*503C>T
ENST00000462306.5:n.374C>T
ENST00000490062.1:n.390C>T
ENST00000494464.5:n.344C>T
ENST00000642308.1:c.460C>T ENSP00000496684.1:p.Gln154Ter
ENST00000644317.1:c.318C>T ENSP00000494012.1:p.Cys106=
ENST00000645233.1:c.460C>T ENSP00000494116.1:p.Gln154Ter
ENST00000645467.1:c.460C>T ENSP00000494889.1:p.Gln154Ter
ENST00000645736.1:c.316C>T ENSP00000494545.1:p.Gln106Ter
ENST00000646654.1:c.460C>T ENSP00000494526.1:p.Gln154Ter
ENST00000647169.1:c.460C>T ENSP00000495619.1:p.Gln154Ter
ENST00000647496.1:c.33C>T
XM_011510794.1:c.460C>T XP_011509096.1:p.Gln154Ter
XM_011510794.2:c.460C>T XP_011509096.1:p.Gln154Ter
XM_011510795.1:c.4C>T XP_011509097.1:p.Gln2Ter
XM_017003583.1:c.4C>T XP_016859072.1:p.Gln2Ter