Canonical Allele Identifier: CA428615977

Gene: ERCC3

Linked Data

• gnomAD v4: 2-127292799-T-C
• MyVariant Identifiers: chr2:g.128050375T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127292799T>C , CM000664.2:g.127292799T>C	GRCh38
NC_000002.11:g.128050375T>C , CM000664.1:g.128050375T>C	GRCh37
NC_000002.10:g.127766845T>C	NCBI36
NG_007454.1:g.6378A>G , LRG_462:g.6378A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285398.7:c.282A>G MANE Select	ENSP00000285398.2:p.Lys94=
ENST00000642308.1:c.282A>G	ENSP00000496684.1:p.Lys94=
ENST00000644317.1:c.235-95A>G	ENSP00000494012.1:n.235-95A>G
ENST00000645233.1:c.282A>G	ENSP00000494116.1:p.Lys94=
ENST00000645467.1:c.282A>G	ENSP00000494889.1:p.Lys94=
ENST00000645736.1:c.138A>G	ENSP00000494545.1:p.Lys46=
ENST00000646654.1:c.282A>G	ENSP00000494526.1:p.Lys94=
ENST00000647169.1:c.282A>G	ENSP00000495619.1:p.Lys94=
ENST00000285398.6:c.282A>G	ENSP00000285398.2:p.Lys94=
ENST00000426778.5:c.*263A>G	ENSP00000415335.1:n.*263A>G
ENST00000445889.5:c.*325A>G	ENSP00000390888.1:n.*325A>G
ENST00000462306.5:n.291-95A>G
ENST00000490062.1:n.307-95A>G
ENST00000494464.5:n.261-95A>G
NM_000122.1:c.282A>G , LRG_462t1:c.282A>G	NP_000113.1:p.Lys94=
NM_001303416.1:c.90A>G	NP_001290345.1:p.Lys30=
NM_001303418.1:c.90A>G	NP_001290347.1:p.Lys30=
XM_011510794.1:c.282A>G	XP_011509096.1:p.Lys94=
XM_011510795.1:c.-80-95A>G	XP_011509097.1:n.-80-95A>G
XM_011510794.2:c.282A>G	XP_011509096.1:p.Lys94=
XM_017003583.1:c.-80-95A>G	XP_016859072.1:n.-80-95A>G
NM_000122.2:c.282A>G MANE Select	NP_000113.1:p.Lys94=
NM_001303416.2:c.90A>G	NP_001290345.1:p.Lys30=
NM_001303418.2:c.90A>G	NP_001290347.1:p.Lys30=