Canonical Allele Identifier: CA2209073542

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13935720G= , CM000678.2:g.13935720G=	GRCh38
NC_000016.9:g.14029577G= , CM000678.1:g.14029577G=	GRCh37
NC_000016.8:g.13937078G=	NCBI36
NG_011442.1:g.20564G= , LRG_463:g.20564G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682568.1:n.1866G=
ENST00000682617.1:c.1926G=	ENSP00000507912.1:p.Ala642=
ENST00000682826.1:c.*1102G=	ENSP00000507274.1:n.*1102G=
ENST00000682909.1:n.3828G=
ENST00000683277.1:n.3433G=
ENST00000683407.1:n.1796G=
ENST00000683962.1:c.*1482G=	ENSP00000506854.1:n.*1482G=
ENST00000311895.8:c.1788G= MANE Select	ENSP00000310520.7:p.Ala596=
ENST00000311895.7:c.1788G=	ENSP00000310520.7:p.Ala596=
ENST00000389138.7:n.1065G=
NM_005236.2:c.1788G= , LRG_463t1:c.1788G=	NP_005227.1:p.Ala596=
XM_011522424.1:c.1926G=	XP_011520726.1:p.Ala642=
XM_011522425.1:c.1245G=	XP_011520727.1:p.Ala415=
XM_011522426.1:c.999G=	XP_011520728.1:p.Ala333=
XM_011522427.1:c.438G=	XP_011520729.1:p.Ala146=
XR_932805.1:n.1947G=
XM_011522424.3:c.1926G=	XP_011520726.1:p.Ala642=
XM_017023043.2:c.999G=	XP_016878532.1:p.Ala333=
NM_005236.3:c.1788G= MANE Select	NP_005227.1:p.Ala596=