Canonical Allele Identifier: CA3222146694

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13947803T= , CM000678.2:g.13947803T=	GRCh38
NC_000016.9:g.14041660T= , CM000678.1:g.14041660T=	GRCh37
NC_000016.8:g.13949161T=	NCBI36
NG_011442.1:g.32647T= , LRG_463:g.32647T=

Transcript Alleles

HGVS	Amino-acid Change
NM_005236.3:c.2207T= MANE Select	NP_005227.1:p.Leu736=
ENST00000311895.8:c.2207T= MANE Select	ENSP00000310520.7:p.Leu736=
NM_005236.2:c.2207T= , LRG_463t1:c.2207T=	NP_005227.1:p.Leu736=
ENST00000311895.7:c.2207T=	ENSP00000310520.7:p.Leu736=
ENST00000389138.7:n.1484T=
ENST00000462862.1:c.520T=	ENSP00000461322.1:n.520T=
ENST00000682617.1:c.2345T=	ENSP00000507912.1:p.Leu782=
ENST00000683962.1:c.*1901T=	ENSP00000506854.1:n.*1901T=
XM_011522424.1:c.2345T=	XP_011520726.1:p.Leu782=
XM_011522424.3:c.2345T=	XP_011520726.1:p.Leu782=
XM_011522425.1:c.1664T=	XP_011520727.1:p.Leu555=
XM_011522426.1:c.1418T=	XP_011520728.1:p.Leu473=
XM_011522427.1:c.857T=	XP_011520729.1:p.Leu286=
XM_017023043.2:c.1418T=	XP_016878532.1:p.Leu473=
XR_932805.1:n.2366T=