Canonical Allele Identifier: CA1286822692

Gene: ERCC3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127292623A= , CM000664.2:g.127292623A=	GRCh38
NC_000002.11:g.128050199A= , CM000664.1:g.128050199A=	GRCh37
NC_000002.10:g.127766669A=	NCBI36
NG_007454.1:g.6554T= , LRG_462:g.6554T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285398.7:c.458T= MANE Select	ENSP00000285398.2:p.Met153=
ENST00000642308.1:c.458T=	ENSP00000496684.1:p.Met153=
ENST00000644317.1:c.316T=	ENSP00000494012.1:p.Cys106=
ENST00000645233.1:c.458T=	ENSP00000494116.1:p.Met153=
ENST00000645467.1:c.458T=	ENSP00000494889.1:p.Met153=
ENST00000645736.1:c.314T=	ENSP00000494545.1:p.Met105=
ENST00000646654.1:c.458T=	ENSP00000494526.1:p.Met153=
ENST00000647169.1:c.458T=	ENSP00000495619.1:p.Met153=
ENST00000647496.1:c.31T=
ENST00000285398.6:c.458T=	ENSP00000285398.2:p.Met153=
ENST00000426778.5:c.*439T=	ENSP00000415335.1:n.*439T=
ENST00000445889.5:c.*501T=	ENSP00000390888.1:n.*501T=
ENST00000462306.5:n.372T=
ENST00000490062.1:n.388T=
ENST00000494464.5:n.342T=
NM_000122.1:c.458T= , LRG_462t1:c.458T=	NP_000113.1:p.Met153=
NM_001303416.1:c.266T=	NP_001290345.1:p.Met89=
NM_001303418.1:c.266T=	NP_001290347.1:p.Met89=
XM_011510794.1:c.458T=	XP_011509096.1:p.Met153=
XM_011510795.1:c.2T=	XP_011509097.1:p.Met1=
XM_011510794.2:c.458T=	XP_011509096.1:p.Met153=
XM_017003583.1:c.2T=	XP_016859072.1:p.Met1=
NM_000122.2:c.458T= MANE Select	NP_000113.1:p.Met153=
NM_001303416.2:c.266T=	NP_001290345.1:p.Met89=
NM_001303418.2:c.266T=	NP_001290347.1:p.Met89=