Canonical Allele Identifier: CA2209082809

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13947977A= , CM000678.2:g.13947977A=	GRCh38
NC_000016.9:g.14041834A= , CM000678.1:g.14041834A=	GRCh37
NC_000016.8:g.13949335A=	NCBI36
NG_011442.1:g.32821A= , LRG_463:g.32821A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2519A=	ENSP00000507912.1:p.His840=
ENST00000683962.1:c.*2075A=	ENSP00000506854.1:n.*2075A=
ENST00000311895.8:c.2381A= MANE Select	ENSP00000310520.7:p.His794=
ENST00000311895.7:c.2381A=	ENSP00000310520.7:p.His794=
ENST00000389138.7:n.1658A=
ENST00000462862.1:c.694A=	ENSP00000461322.1:n.694A=
NM_005236.2:c.2381A= , LRG_463t1:c.2381A=	NP_005227.1:p.His794=
XM_011522424.1:c.2519A=	XP_011520726.1:p.His840=
XM_011522425.1:c.1838A=	XP_011520727.1:p.His613=
XM_011522426.1:c.1592A=	XP_011520728.1:p.His531=
XM_011522427.1:c.1031A=	XP_011520729.1:p.His344=
XR_932805.1:n.2540A=
XM_011522424.3:c.2519A=	XP_011520726.1:p.His840=
XM_017023043.2:c.1592A=	XP_016878532.1:p.His531=
NM_005236.3:c.2381A= MANE Select	NP_005227.1:p.His794=