Canonical Allele Identifier: CA2209082795

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13947956A= , CM000678.2:g.13947956A=	GRCh38
NC_000016.9:g.14041813A= , CM000678.1:g.14041813A=	GRCh37
NC_000016.8:g.13949314A=	NCBI36
NG_011442.1:g.32800A= , LRG_463:g.32800A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2498A=	ENSP00000507912.1:p.Lys833=
ENST00000683962.1:c.*2054A=	ENSP00000506854.1:n.*2054A=
ENST00000311895.8:c.2360A= MANE Select	ENSP00000310520.7:p.Lys787=
ENST00000311895.7:c.2360A=	ENSP00000310520.7:p.Lys787=
ENST00000389138.7:n.1637A=
ENST00000462862.1:c.673A=	ENSP00000461322.1:n.673A=
NM_005236.2:c.2360A= , LRG_463t1:c.2360A=	NP_005227.1:p.Lys787=
XM_011522424.1:c.2498A=	XP_011520726.1:p.Lys833=
XM_011522425.1:c.1817A=	XP_011520727.1:p.Lys606=
XM_011522426.1:c.1571A=	XP_011520728.1:p.Lys524=
XM_011522427.1:c.1010A=	XP_011520729.1:p.Lys337=
XR_932805.1:n.2519A=
XM_011522424.3:c.2498A=	XP_011520726.1:p.Lys833=
XM_017023043.2:c.1571A=	XP_016878532.1:p.Lys524=
NM_005236.3:c.2360A= MANE Select	NP_005227.1:p.Lys787=