Canonical Allele Identifier: CA2209082933

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13948237C= , CM000678.2:g.13948237C=	GRCh38
NC_000016.9:g.14042094C= , CM000678.1:g.14042094C=	GRCh37
NC_000016.8:g.13949595C=	NCBI36
NG_011442.1:g.33081C= , LRG_463:g.33081C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682617.1:c.2779C=	ENSP00000507912.1:p.Gln927=
ENST00000683962.1:c.*2335C=	ENSP00000506854.1:n.*2335C=
ENST00000311895.8:c.2641C= MANE Select	ENSP00000310520.7:p.Gln881=
ENST00000311895.7:c.2641C=	ENSP00000310520.7:p.Gln881=
ENST00000389138.7:n.1918C=
NM_005236.2:c.2641C= , LRG_463t1:c.2641C=	NP_005227.1:p.Gln881=
XM_011522424.1:c.2779C=	XP_011520726.1:p.Gln927=
XM_011522425.1:c.2098C=	XP_011520727.1:p.Gln700=
XM_011522426.1:c.1852C=	XP_011520728.1:p.Gln618=
XM_011522427.1:c.1291C=	XP_011520729.1:p.Gln431=
XR_932805.1:n.2800C=
XM_011522424.3:c.2779C=	XP_011520726.1:p.Gln927=
XM_017023043.2:c.1852C=	XP_016878532.1:p.Gln618=
NM_005236.3:c.2641C= MANE Select	NP_005227.1:p.Gln881=