Canonical Allele Identifier: CA1286822709

Gene: ERCC3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127292669_127292670delinsCG , CM000664.2:g.127292669_127292670delinsCG	GRCh38
NC_000002.11:g.128050245_128050246delinsCG , CM000664.1:g.128050245_128050246delinsCG	GRCh37
NC_000002.10:g.127766715_127766716delinsCG	NCBI36
NG_007454.1:g.6507_6508delinsCG , LRG_462:g.6507_6508delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285398.7:c.411_412delinsCG MANE Select	ENSP00000285398.2:p.Thr137=
ENST00000642308.1:c.411_412delinsCG	ENSP00000496684.1:p.Thr137=
ENST00000644317.1:c.269_270delinsCG	ENSP00000494012.1:p.Pro90=
ENST00000645233.1:c.411_412delinsCG	ENSP00000494116.1:p.Thr137=
ENST00000645467.1:c.411_412delinsCG	ENSP00000494889.1:p.Thr137=
ENST00000645736.1:c.267_268delinsCG	ENSP00000494545.1:p.Thr89=
ENST00000646654.1:c.411_412delinsCG	ENSP00000494526.1:p.Thr137=
ENST00000647169.1:c.411_412delinsCG	ENSP00000495619.1:p.Thr137=
ENST00000285398.6:c.411_412delinsCG	ENSP00000285398.2:p.Thr137=
ENST00000426778.5:c.*392_*393delinsCG	ENSP00000415335.1:n.*392_*393delinsCG
ENST00000445889.5:c.*454_*455delinsCG	ENSP00000390888.1:n.*454_*455delinsCG
ENST00000462306.5:n.325_326delinsCG
ENST00000490062.1:n.341_342delinsCG
ENST00000494464.5:n.295_296delinsCG
NM_000122.1:c.411_412delinsCG , LRG_462t1:c.411_412delinsCG	NP_000113.1:p.Thr137=
NM_001303416.1:c.219_220delinsCG	NP_001290345.1:p.Thr73=
NM_001303418.1:c.219_220delinsCG	NP_001290347.1:p.Thr73=
XM_011510794.1:c.411_412delinsCG	XP_011509096.1:p.Thr137=
XM_011510795.1:c.-46_-45delinsCG	XP_011509097.1:n.-46_-45delinsCG
XM_011510794.2:c.411_412delinsCG	XP_011509096.1:p.Thr137=
XM_017003583.1:c.-46_-45delinsCG	XP_016859072.1:n.-46_-45delinsCG
NM_000122.2:c.411_412delinsCG MANE Select	NP_000113.1:p.Thr137=
NM_001303416.2:c.219_220delinsCG	NP_001290345.1:p.Thr73=
NM_001303418.2:c.219_220delinsCG	NP_001290347.1:p.Thr73=