Canonical Allele Identifier: CA2209082919

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13948211A= , CM000678.2:g.13948211A=	GRCh38
NC_000016.9:g.14042068A= , CM000678.1:g.14042068A=	GRCh37
NC_000016.8:g.13949569A=	NCBI36
NG_011442.1:g.33055A= , LRG_463:g.33055A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2753A=	ENSP00000507912.1:p.Asn918=
ENST00000683962.1:c.*2309A=	ENSP00000506854.1:n.*2309A=
ENST00000311895.8:c.2615A= MANE Select	ENSP00000310520.7:p.Asn872=
ENST00000311895.7:c.2615A=	ENSP00000310520.7:p.Asn872=
ENST00000389138.7:n.1892A=
NM_005236.2:c.2615A= , LRG_463t1:c.2615A=	NP_005227.1:p.Asn872=
XM_011522424.1:c.2753A=	XP_011520726.1:p.Asn918=
XM_011522425.1:c.2072A=	XP_011520727.1:p.Asn691=
XM_011522426.1:c.1826A=	XP_011520728.1:p.Asn609=
XM_011522427.1:c.1265A=	XP_011520729.1:p.Asn422=
XR_932805.1:n.2774A=
XM_011522424.3:c.2753A=	XP_011520726.1:p.Asn918=
XM_017023043.2:c.1826A=	XP_016878532.1:p.Asn609=
NM_005236.3:c.2615A= MANE Select	NP_005227.1:p.Asn872=