Canonical Allele Identifier: CA2209082921

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13948213A= , CM000678.2:g.13948213A=	GRCh38
NC_000016.9:g.14042070A= , CM000678.1:g.14042070A=	GRCh37
NC_000016.8:g.13949571A=	NCBI36
NG_011442.1:g.33057A= , LRG_463:g.33057A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2755A=	ENSP00000507912.1:p.Ile919=
ENST00000683962.1:c.*2311A=	ENSP00000506854.1:n.*2311A=
ENST00000311895.8:c.2617A= MANE Select	ENSP00000310520.7:p.Ile873=
ENST00000311895.7:c.2617A=	ENSP00000310520.7:p.Ile873=
ENST00000389138.7:n.1894A=
NM_005236.2:c.2617A= , LRG_463t1:c.2617A=	NP_005227.1:p.Ile873=
XM_011522424.1:c.2755A=	XP_011520726.1:p.Ile919=
XM_011522425.1:c.2074A=	XP_011520727.1:p.Ile692=
XM_011522426.1:c.1828A=	XP_011520728.1:p.Ile610=
XM_011522427.1:c.1267A=	XP_011520729.1:p.Ile423=
XR_932805.1:n.2776A=
XM_011522424.3:c.2755A=	XP_011520726.1:p.Ile919=
XM_017023043.2:c.1828A=	XP_016878532.1:p.Ile610=
NM_005236.3:c.2617A= MANE Select	NP_005227.1:p.Ile873=