Canonical Allele Identifier: CA1286822770

Gene: ERCC3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127292818G= , CM000664.2:g.127292818G=	GRCh38
NC_000002.11:g.128050394G= , CM000664.1:g.128050394G=	GRCh37
NC_000002.10:g.127766864G=	NCBI36
NG_007454.1:g.6359C= , LRG_462:g.6359C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285398.7:c.263C= MANE Select	ENSP00000285398.2:p.Ala88=
ENST00000642308.1:c.263C=	ENSP00000496684.1:p.Ala88=
ENST00000644317.1:c.235-114C=	ENSP00000494012.1:n.235-114C=
ENST00000645233.1:c.263C=	ENSP00000494116.1:p.Ala88=
ENST00000645467.1:c.263C=	ENSP00000494889.1:p.Ala88=
ENST00000645736.1:c.119C=	ENSP00000494545.1:p.Ala40=
ENST00000646654.1:c.263C=	ENSP00000494526.1:p.Ala88=
ENST00000647169.1:c.263C=	ENSP00000495619.1:p.Ala88=
ENST00000285398.6:c.263C=	ENSP00000285398.2:p.Ala88=
ENST00000426778.5:c.*244C=	ENSP00000415335.1:n.*244C=
ENST00000445889.5:c.*306C=	ENSP00000390888.1:n.*306C=
ENST00000462306.5:n.291-114C=
ENST00000490062.1:n.307-114C=
ENST00000494464.5:n.261-114C=
NM_000122.1:c.263C= , LRG_462t1:c.263C=	NP_000113.1:p.Ala88=
NM_001303416.1:c.71C=	NP_001290345.1:p.Ala24=
NM_001303418.1:c.71C=	NP_001290347.1:p.Ala24=
XM_011510794.1:c.263C=	XP_011509096.1:p.Ala88=
XM_011510795.1:c.-80-114C=	XP_011509097.1:n.-80-114C=
XM_011510794.2:c.263C=	XP_011509096.1:p.Ala88=
XM_017003583.1:c.-80-114C=	XP_016859072.1:n.-80-114C=
NM_000122.2:c.263C= MANE Select	NP_000113.1:p.Ala88=
NM_001303416.2:c.71C=	NP_001290345.1:p.Ala24=
NM_001303418.2:c.71C=	NP_001290347.1:p.Ala24=