Canonical Allele Identifier: CA2209082843

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13948048C= , CM000678.2:g.13948048C=	GRCh38
NC_000016.9:g.14041905C= , CM000678.1:g.14041905C=	GRCh37
NC_000016.8:g.13949406C=	NCBI36
NG_011442.1:g.32892C= , LRG_463:g.32892C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2590C=	ENSP00000507912.1:p.Gln864=
ENST00000683962.1:c.*2146C=	ENSP00000506854.1:n.*2146C=
ENST00000311895.8:c.2452C= MANE Select	ENSP00000310520.7:p.Gln818=
ENST00000311895.7:c.2452C=	ENSP00000310520.7:p.Gln818=
ENST00000389138.7:n.1729C=
NM_005236.2:c.2452C= , LRG_463t1:c.2452C=	NP_005227.1:p.Gln818=
XM_011522424.1:c.2590C=	XP_011520726.1:p.Gln864=
XM_011522425.1:c.1909C=	XP_011520727.1:p.Gln637=
XM_011522426.1:c.1663C=	XP_011520728.1:p.Gln555=
XM_011522427.1:c.1102C=	XP_011520729.1:p.Gln368=
XR_932805.1:n.2611C=
XM_011522424.3:c.2590C=	XP_011520726.1:p.Gln864=
XM_017023043.2:c.1663C=	XP_016878532.1:p.Gln555=
NM_005236.3:c.2452C= MANE Select	NP_005227.1:p.Gln818=