Canonical Allele Identifier: CA2209082837

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13948032G= , CM000678.2:g.13948032G=	GRCh38
NC_000016.9:g.14041889G= , CM000678.1:g.14041889G=	GRCh37
NC_000016.8:g.13949390G=	NCBI36
NG_011442.1:g.32876G= , LRG_463:g.32876G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682617.1:c.2574G=	ENSP00000507912.1:p.Leu858=
ENST00000683962.1:c.*2130G=	ENSP00000506854.1:n.*2130G=
ENST00000311895.8:c.2436G= MANE Select	ENSP00000310520.7:p.Leu812=
ENST00000311895.7:c.2436G=	ENSP00000310520.7:p.Leu812=
ENST00000389138.7:n.1713G=
NM_005236.2:c.2436G= , LRG_463t1:c.2436G=	NP_005227.1:p.Leu812=
XM_011522424.1:c.2574G=	XP_011520726.1:p.Leu858=
XM_011522425.1:c.1893G=	XP_011520727.1:p.Leu631=
XM_011522426.1:c.1647G=	XP_011520728.1:p.Leu549=
XM_011522427.1:c.1086G=	XP_011520729.1:p.Leu362=
XR_932805.1:n.2595G=
XM_011522424.3:c.2574G=	XP_011520726.1:p.Leu858=
XM_017023043.2:c.1647G=	XP_016878532.1:p.Leu549=
NM_005236.3:c.2436G= MANE Select	NP_005227.1:p.Leu812=