Canonical Allele Identifier: CA2209082730

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13947828G= , CM000678.2:g.13947828G=	GRCh38
NC_000016.9:g.14041685G= , CM000678.1:g.14041685G=	GRCh37
NC_000016.8:g.13949186G=	NCBI36
NG_011442.1:g.32672G= , LRG_463:g.32672G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682617.1:c.2370G=	ENSP00000507912.1:p.Gln790=
ENST00000683962.1:c.*1926G=	ENSP00000506854.1:n.*1926G=
ENST00000311895.8:c.2232G= MANE Select	ENSP00000310520.7:p.Gln744=
ENST00000311895.7:c.2232G=	ENSP00000310520.7:p.Gln744=
ENST00000389138.7:n.1509G=
ENST00000462862.1:c.545G=	ENSP00000461322.1:n.545G=
NM_005236.2:c.2232G= , LRG_463t1:c.2232G=	NP_005227.1:p.Gln744=
XM_011522424.1:c.2370G=	XP_011520726.1:p.Gln790=
XM_011522425.1:c.1689G=	XP_011520727.1:p.Gln563=
XM_011522426.1:c.1443G=	XP_011520728.1:p.Gln481=
XM_011522427.1:c.882G=	XP_011520729.1:p.Gln294=
XR_932805.1:n.2391G=
XM_011522424.3:c.2370G=	XP_011520726.1:p.Gln790=
XM_017023043.2:c.1443G=	XP_016878532.1:p.Gln481=
NM_005236.3:c.2232G= MANE Select	NP_005227.1:p.Gln744=