Canonical Allele Identifier: CA2209082742

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13947851A= , CM000678.2:g.13947851A=	GRCh38
NC_000016.9:g.14041708A= , CM000678.1:g.14041708A=	GRCh37
NC_000016.8:g.13949209A=	NCBI36
NG_011442.1:g.32695A= , LRG_463:g.32695A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2393A=	ENSP00000507912.1:p.Tyr798=
ENST00000683962.1:c.*1949A=	ENSP00000506854.1:n.*1949A=
ENST00000311895.8:c.2255A= MANE Select	ENSP00000310520.7:p.Tyr752=
ENST00000311895.7:c.2255A=	ENSP00000310520.7:p.Tyr752=
ENST00000389138.7:n.1532A=
ENST00000462862.1:c.568A=	ENSP00000461322.1:n.568A=
NM_005236.2:c.2255A= , LRG_463t1:c.2255A=	NP_005227.1:p.Tyr752=
XM_011522424.1:c.2393A=	XP_011520726.1:p.Tyr798=
XM_011522425.1:c.1712A=	XP_011520727.1:p.Tyr571=
XM_011522426.1:c.1466A=	XP_011520728.1:p.Tyr489=
XM_011522427.1:c.905A=	XP_011520729.1:p.Tyr302=
XR_932805.1:n.2414A=
XM_011522424.3:c.2393A=	XP_011520726.1:p.Tyr798=
XM_017023043.2:c.1466A=	XP_016878532.1:p.Tyr489=
NM_005236.3:c.2255A= MANE Select	NP_005227.1:p.Tyr752=