Canonical Allele Identifier: CA2209082874

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13948131T= , CM000678.2:g.13948131T=	GRCh38
NC_000016.9:g.14041988T= , CM000678.1:g.14041988T=	GRCh37
NC_000016.8:g.13949489T=	NCBI36
NG_011442.1:g.32975T= , LRG_463:g.32975T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2673T=	ENSP00000507912.1:p.Asn891=
ENST00000683962.1:c.*2229T=	ENSP00000506854.1:n.*2229T=
ENST00000311895.8:c.2535T= MANE Select	ENSP00000310520.7:p.Asn845=
ENST00000311895.7:c.2535T=	ENSP00000310520.7:p.Asn845=
ENST00000389138.7:n.1812T=
NM_005236.2:c.2535T= , LRG_463t1:c.2535T=	NP_005227.1:p.Asn845=
XM_011522424.1:c.2673T=	XP_011520726.1:p.Asn891=
XM_011522425.1:c.1992T=	XP_011520727.1:p.Asn664=
XM_011522426.1:c.1746T=	XP_011520728.1:p.Asn582=
XM_011522427.1:c.1185T=	XP_011520729.1:p.Asn395=
XR_932805.1:n.2694T=
XM_011522424.3:c.2673T=	XP_011520726.1:p.Asn891=
XM_017023043.2:c.1746T=	XP_016878532.1:p.Asn582=
NM_005236.3:c.2535T= MANE Select	NP_005227.1:p.Asn845=