Canonical Allele Identifier: CA2209082929

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13948228G= , CM000678.2:g.13948228G=	GRCh38
NC_000016.9:g.14042085G= , CM000678.1:g.14042085G=	GRCh37
NC_000016.8:g.13949586G=	NCBI36
NG_011442.1:g.33072G= , LRG_463:g.33072G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682617.1:c.2770G=	ENSP00000507912.1:p.Ala924=
ENST00000683962.1:c.*2326G=	ENSP00000506854.1:n.*2326G=
ENST00000311895.8:c.2632G= MANE Select	ENSP00000310520.7:p.Ala878=
ENST00000311895.7:c.2632G=	ENSP00000310520.7:p.Ala878=
ENST00000389138.7:n.1909G=
NM_005236.2:c.2632G= , LRG_463t1:c.2632G=	NP_005227.1:p.Ala878=
XM_011522424.1:c.2770G=	XP_011520726.1:p.Ala924=
XM_011522425.1:c.2089G=	XP_011520727.1:p.Ala697=
XM_011522426.1:c.1843G=	XP_011520728.1:p.Ala615=
XM_011522427.1:c.1282G=	XP_011520729.1:p.Ala428=
XR_932805.1:n.2791G=
XM_011522424.3:c.2770G=	XP_011520726.1:p.Ala924=
XM_017023043.2:c.1843G=	XP_016878532.1:p.Ala615=
NM_005236.3:c.2632G= MANE Select	NP_005227.1:p.Ala878=