Canonical Allele Identifier: CA2209082676

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13947704G= , CM000678.2:g.13947704G=	GRCh38
NC_000016.9:g.14041561G= , CM000678.1:g.14041561G=	GRCh37
NC_000016.8:g.13949062G=	NCBI36
NG_011442.1:g.32548G= , LRG_463:g.32548G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2246G=	ENSP00000507912.1:p.Gly749=
ENST00000683962.1:c.*1802G=	ENSP00000506854.1:n.*1802G=
ENST00000311895.8:c.2108G= MANE Select	ENSP00000310520.7:p.Gly703=
ENST00000311895.7:c.2108G=	ENSP00000310520.7:p.Gly703=
ENST00000389138.7:n.1385G=
ENST00000462862.1:c.421G=	ENSP00000461322.1:n.421G=
NM_005236.2:c.2108G= , LRG_463t1:c.2108G=	NP_005227.1:p.Gly703=
XM_011522424.1:c.2246G=	XP_011520726.1:p.Gly749=
XM_011522425.1:c.1565G=	XP_011520727.1:p.Gly522=
XM_011522426.1:c.1319G=	XP_011520728.1:p.Gly440=
XM_011522427.1:c.758G=	XP_011520729.1:p.Gly253=
XR_932805.1:n.2267G=
XM_011522424.3:c.2246G=	XP_011520726.1:p.Gly749=
XM_017023043.2:c.1319G=	XP_016878532.1:p.Gly440=
NM_005236.3:c.2108G= MANE Select	NP_005227.1:p.Gly703=