Canonical Allele Identifier: CA2209082848

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13948061A= , CM000678.2:g.13948061A=	GRCh38
NC_000016.9:g.14041918A= , CM000678.1:g.14041918A=	GRCh37
NC_000016.8:g.13949419A=	NCBI36
NG_011442.1:g.32905A= , LRG_463:g.32905A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2603A=	ENSP00000507912.1:p.Gln868=
ENST00000683962.1:c.*2159A=	ENSP00000506854.1:n.*2159A=
ENST00000311895.8:c.2465A= MANE Select	ENSP00000310520.7:p.Gln822=
ENST00000311895.7:c.2465A=	ENSP00000310520.7:p.Gln822=
ENST00000389138.7:n.1742A=
NM_005236.2:c.2465A= , LRG_463t1:c.2465A=	NP_005227.1:p.Gln822=
XM_011522424.1:c.2603A=	XP_011520726.1:p.Gln868=
XM_011522425.1:c.1922A=	XP_011520727.1:p.Gln641=
XM_011522426.1:c.1676A=	XP_011520728.1:p.Gln559=
XM_011522427.1:c.1115A=	XP_011520729.1:p.Gln372=
XR_932805.1:n.2624A=
XM_011522424.3:c.2603A=	XP_011520726.1:p.Gln868=
XM_017023043.2:c.1676A=	XP_016878532.1:p.Gln559=
NM_005236.3:c.2465A= MANE Select	NP_005227.1:p.Gln822=