Canonical Allele Identifier: CA2209082938

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13948248C= , CM000678.2:g.13948248C=	GRCh38
NC_000016.9:g.14042105C= , CM000678.1:g.14042105C=	GRCh37
NC_000016.8:g.13949606C=	NCBI36
NG_011442.1:g.33092C= , LRG_463:g.33092C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682617.1:c.2790C=	ENSP00000507912.1:p.Leu930=
ENST00000683962.1:c.*2346C=	ENSP00000506854.1:n.*2346C=
ENST00000311895.8:c.2652C= MANE Select	ENSP00000310520.7:p.Leu884=
ENST00000311895.7:c.2652C=	ENSP00000310520.7:p.Leu884=
ENST00000389138.7:n.1929C=
NM_005236.2:c.2652C= , LRG_463t1:c.2652C=	NP_005227.1:p.Leu884=
XM_011522424.1:c.2790C=	XP_011520726.1:p.Leu930=
XM_011522425.1:c.2109C=	XP_011520727.1:p.Leu703=
XM_011522426.1:c.1863C=	XP_011520728.1:p.Leu621=
XM_011522427.1:c.1302C=	XP_011520729.1:p.Leu434=
XR_932805.1:n.2811C=
XM_011522424.3:c.2790C=	XP_011520726.1:p.Leu930=
XM_017023043.2:c.1863C=	XP_016878532.1:p.Leu621=
NM_005236.3:c.2652C= MANE Select	NP_005227.1:p.Leu884=