Canonical Allele Identifier: CA2209082768

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13947899C= , CM000678.2:g.13947899C=	GRCh38
NC_000016.9:g.14041756C= , CM000678.1:g.14041756C=	GRCh37
NC_000016.8:g.13949257C=	NCBI36
NG_011442.1:g.32743C= , LRG_463:g.32743C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682617.1:c.2441C=	ENSP00000507912.1:p.Ser814=
ENST00000683962.1:c.*1997C=	ENSP00000506854.1:n.*1997C=
ENST00000311895.8:c.2303C= MANE Select	ENSP00000310520.7:p.Ser768=
ENST00000311895.7:c.2303C=	ENSP00000310520.7:p.Ser768=
ENST00000389138.7:n.1580C=
ENST00000462862.1:c.616C=	ENSP00000461322.1:n.616C=
NM_005236.2:c.2303C= , LRG_463t1:c.2303C=	NP_005227.1:p.Ser768=
XM_011522424.1:c.2441C=	XP_011520726.1:p.Ser814=
XM_011522425.1:c.1760C=	XP_011520727.1:p.Ser587=
XM_011522426.1:c.1514C=	XP_011520728.1:p.Ser505=
XM_011522427.1:c.953C=	XP_011520729.1:p.Ser318=
XR_932805.1:n.2462C=
XM_011522424.3:c.2441C=	XP_011520726.1:p.Ser814=
XM_017023043.2:c.1514C=	XP_016878532.1:p.Ser505=
NM_005236.3:c.2303C= MANE Select	NP_005227.1:p.Ser768=