Canonical Allele Identifier: CA428615879

Gene: ERCC3

Linked Data

• MyVariant Identifiers: chr2:g.128050270A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127292694A>T , CM000664.2:g.127292694A>T	GRCh38
NC_000002.11:g.128050270A>T , CM000664.1:g.128050270A>T	GRCh37
NC_000002.10:g.127766740A>T	NCBI36
NG_007454.1:g.6483T>A , LRG_462:g.6483T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000285398.7:c.387T>A MANE Select	ENSP00000285398.2:p.Val129=
ENST00000642308.1:c.387T>A	ENSP00000496684.1:p.Val129=
ENST00000644317.1:c.245T>A	ENSP00000494012.1:p.Leu82Ter
ENST00000645233.1:c.387T>A	ENSP00000494116.1:p.Val129=
ENST00000645467.1:c.387T>A	ENSP00000494889.1:p.Val129=
ENST00000645736.1:c.243T>A	ENSP00000494545.1:p.Val81=
ENST00000646654.1:c.387T>A	ENSP00000494526.1:p.Val129=
ENST00000647169.1:c.387T>A	ENSP00000495619.1:p.Val129=
ENST00000285398.6:c.387T>A	ENSP00000285398.2:p.Val129=
ENST00000426778.5:c.*368T>A	ENSP00000415335.1:n.*368T>A
ENST00000445889.5:c.*430T>A	ENSP00000390888.1:n.*430T>A
ENST00000462306.5:n.301T>A
ENST00000490062.1:n.317T>A
ENST00000494464.5:n.271T>A
NM_000122.1:c.387T>A , LRG_462t1:c.387T>A	NP_000113.1:p.Val129=
NM_001303416.1:c.195T>A	NP_001290345.1:p.Val65=
NM_001303418.1:c.195T>A	NP_001290347.1:p.Val65=
XM_011510794.1:c.387T>A	XP_011509096.1:p.Val129=
XM_011510795.1:c.-70T>A	XP_011509097.1:n.-70T>A
XM_011510794.2:c.387T>A	XP_011509096.1:p.Val129=
XM_017003583.1:c.-70T>A	XP_016859072.1:n.-70T>A
NM_000122.2:c.387T>A MANE Select	NP_000113.1:p.Val129=
NM_001303416.2:c.195T>A	NP_001290345.1:p.Val65=
NM_001303418.2:c.195T>A	NP_001290347.1:p.Val65=