Canonical Allele Identifier: CA2209082899

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13948181A= , CM000678.2:g.13948181A=	GRCh38
NC_000016.9:g.14042038A= , CM000678.1:g.14042038A=	GRCh37
NC_000016.8:g.13949539A=	NCBI36
NG_011442.1:g.33025A= , LRG_463:g.33025A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2723A=	ENSP00000507912.1:p.Asn908=
ENST00000683962.1:c.*2279A=	ENSP00000506854.1:n.*2279A=
ENST00000311895.8:c.2585A= MANE Select	ENSP00000310520.7:p.Asn862=
ENST00000311895.7:c.2585A=	ENSP00000310520.7:p.Asn862=
ENST00000389138.7:n.1862A=
NM_005236.2:c.2585A= , LRG_463t1:c.2585A=	NP_005227.1:p.Asn862=
XM_011522424.1:c.2723A=	XP_011520726.1:p.Asn908=
XM_011522425.1:c.2042A=	XP_011520727.1:p.Asn681=
XM_011522426.1:c.1796A=	XP_011520728.1:p.Asn599=
XM_011522427.1:c.1235A=	XP_011520729.1:p.Asn412=
XR_932805.1:n.2744A=
XM_011522424.3:c.2723A=	XP_011520726.1:p.Asn908=
XM_017023043.2:c.1796A=	XP_016878532.1:p.Asn599=
NM_005236.3:c.2585A= MANE Select	NP_005227.1:p.Asn862=