Canonical Allele Identifier: CA1286822698

Gene: ERCC3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127292637G= , CM000664.2:g.127292637G=	GRCh38
NC_000002.11:g.128050213G= , CM000664.1:g.128050213G=	GRCh37
NC_000002.10:g.127766683G=	NCBI36
NG_007454.1:g.6540C= , LRG_462:g.6540C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000285398.7:c.444C= MANE Select	ENSP00000285398.2:p.Val148=
ENST00000642308.1:c.444C=	ENSP00000496684.1:p.Val148=
ENST00000644317.1:c.302C=	ENSP00000494012.1:p.Ser101=
ENST00000645233.1:c.444C=	ENSP00000494116.1:p.Val148=
ENST00000645467.1:c.444C=	ENSP00000494889.1:p.Val148=
ENST00000645736.1:c.300C=	ENSP00000494545.1:p.Val100=
ENST00000646654.1:c.444C=	ENSP00000494526.1:p.Val148=
ENST00000647169.1:c.444C=	ENSP00000495619.1:p.Val148=
ENST00000647496.1:c.17C=
ENST00000285398.6:c.444C=	ENSP00000285398.2:p.Val148=
ENST00000426778.5:c.*425C=	ENSP00000415335.1:n.*425C=
ENST00000445889.5:c.*487C=	ENSP00000390888.1:n.*487C=
ENST00000462306.5:n.358C=
ENST00000490062.1:n.374C=
ENST00000494464.5:n.328C=
NM_000122.1:c.444C= , LRG_462t1:c.444C=	NP_000113.1:p.Val148=
NM_001303416.1:c.252C=	NP_001290345.1:p.Val84=
NM_001303418.1:c.252C=	NP_001290347.1:p.Val84=
XM_011510794.1:c.444C=	XP_011509096.1:p.Val148=
XM_011510795.1:c.-13C=	XP_011509097.1:n.-13C=
XM_011510794.2:c.444C=	XP_011509096.1:p.Val148=
XM_017003583.1:c.-13C=	XP_016859072.1:n.-13C=
NM_000122.2:c.444C= MANE Select	NP_000113.1:p.Val148=
NM_001303416.2:c.252C=	NP_001290345.1:p.Val84=
NM_001303418.2:c.252C=	NP_001290347.1:p.Val84=