Canonical Allele Identifier: CA2209073333

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13935608G= , CM000678.2:g.13935608G=	GRCh38
NC_000016.9:g.14029465G= , CM000678.1:g.14029465G=	GRCh37
NC_000016.8:g.13936966G=	NCBI36
NG_011442.1:g.20452G= , LRG_463:g.20452G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682568.1:n.1754G=
ENST00000682617.1:c.1814G=	ENSP00000507912.1:p.Gly605=
ENST00000682826.1:c.*990G=	ENSP00000507274.1:n.*990G=
ENST00000682909.1:n.3716G=
ENST00000683277.1:n.3321G=
ENST00000683407.1:n.1684G=
ENST00000683962.1:c.*1370G=	ENSP00000506854.1:n.*1370G=
ENST00000311895.8:c.1676G= MANE Select	ENSP00000310520.7:p.Gly559=
ENST00000311895.7:c.1676G=	ENSP00000310520.7:p.Gly559=
ENST00000389138.7:n.953G=
NM_005236.2:c.1676G= , LRG_463t1:c.1676G=	NP_005227.1:p.Gly559=
XM_011522424.1:c.1814G=	XP_011520726.1:p.Gly605=
XM_011522425.1:c.1133G=	XP_011520727.1:p.Gly378=
XM_011522426.1:c.887G=	XP_011520728.1:p.Gly296=
XM_011522427.1:c.326G=	XP_011520729.1:p.Gly109=
XR_932805.1:n.1835G=
XM_011522424.3:c.1814G=	XP_011520726.1:p.Gly605=
XM_017023043.2:c.887G=	XP_016878532.1:p.Gly296=
NM_005236.3:c.1676G= MANE Select	NP_005227.1:p.Gly559=