Canonical Allele Identifier: CA2209082825

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13948017T= , CM000678.2:g.13948017T=	GRCh38
NC_000016.9:g.14041874T= , CM000678.1:g.14041874T=	GRCh37
NC_000016.8:g.13949375T=	NCBI36
NG_011442.1:g.32861T= , LRG_463:g.32861T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2559T=	ENSP00000507912.1:p.His853=
ENST00000683962.1:c.*2115T=	ENSP00000506854.1:n.*2115T=
ENST00000311895.8:c.2421T= MANE Select	ENSP00000310520.7:p.His807=
ENST00000311895.7:c.2421T=	ENSP00000310520.7:p.His807=
ENST00000389138.7:n.1698T=
NM_005236.2:c.2421T= , LRG_463t1:c.2421T=	NP_005227.1:p.His807=
XM_011522424.1:c.2559T=	XP_011520726.1:p.His853=
XM_011522425.1:c.1878T=	XP_011520727.1:p.His626=
XM_011522426.1:c.1632T=	XP_011520728.1:p.His544=
XM_011522427.1:c.1071T=	XP_011520729.1:p.His357=
XR_932805.1:n.2580T=
XM_011522424.3:c.2559T=	XP_011520726.1:p.His853=
XM_017023043.2:c.1632T=	XP_016878532.1:p.His544=
NM_005236.3:c.2421T= MANE Select	NP_005227.1:p.His807=