Canonical Allele Identifier: CA1286822694

Gene: ERCC3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127292627T= , CM000664.2:g.127292627T=	GRCh38
NC_000002.11:g.128050203T= , CM000664.1:g.128050203T=	GRCh37
NC_000002.10:g.127766673T=	NCBI36
NG_007454.1:g.6550A= , LRG_462:g.6550A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000285398.7:c.454A= MANE Select	ENSP00000285398.2:p.Ile152=
ENST00000642308.1:c.454A=	ENSP00000496684.1:p.Ile152=
ENST00000644317.1:c.312A=	ENSP00000494012.1:p.Glu104=
ENST00000645233.1:c.454A=	ENSP00000494116.1:p.Ile152=
ENST00000645467.1:c.454A=	ENSP00000494889.1:p.Ile152=
ENST00000645736.1:c.310A=	ENSP00000494545.1:p.Ile104=
ENST00000646654.1:c.454A=	ENSP00000494526.1:p.Ile152=
ENST00000647169.1:c.454A=	ENSP00000495619.1:p.Ile152=
ENST00000647496.1:c.27A=
ENST00000285398.6:c.454A=	ENSP00000285398.2:p.Ile152=
ENST00000426778.5:c.*435A=	ENSP00000415335.1:n.*435A=
ENST00000445889.5:c.*497A=	ENSP00000390888.1:n.*497A=
ENST00000462306.5:n.368A=
ENST00000490062.1:n.384A=
ENST00000494464.5:n.338A=
NM_000122.1:c.454A= , LRG_462t1:c.454A=	NP_000113.1:p.Ile152=
NM_001303416.1:c.262A=	NP_001290345.1:p.Ile88=
NM_001303418.1:c.262A=	NP_001290347.1:p.Ile88=
XM_011510794.1:c.454A=	XP_011509096.1:p.Ile152=
XM_011510795.1:c.-3A=	XP_011509097.1:n.-3A=
XM_011510794.2:c.454A=	XP_011509096.1:p.Ile152=
XM_017003583.1:c.-3A=	XP_016859072.1:n.-3A=
NM_000122.2:c.454A= MANE Select	NP_000113.1:p.Ile152=
NM_001303416.2:c.262A=	NP_001290345.1:p.Ile88=
NM_001303418.2:c.262A=	NP_001290347.1:p.Ile88=