Canonical Allele Identifier: CA2209073320

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13935599C= , CM000678.2:g.13935599C=	GRCh38
NC_000016.9:g.14029456C= , CM000678.1:g.14029456C=	GRCh37
NC_000016.8:g.13936957C=	NCBI36
NG_011442.1:g.20443C= , LRG_463:g.20443C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682568.1:n.1745C=
ENST00000682617.1:c.1805C=	ENSP00000507912.1:p.Pro602=
ENST00000682826.1:c.*981C=	ENSP00000507274.1:n.*981C=
ENST00000682909.1:n.3707C=
ENST00000683277.1:n.3312C=
ENST00000683407.1:n.1675C=
ENST00000683962.1:c.*1361C=	ENSP00000506854.1:n.*1361C=
ENST00000311895.8:c.1667C= MANE Select	ENSP00000310520.7:p.Pro556=
ENST00000311895.7:c.1667C=	ENSP00000310520.7:p.Pro556=
ENST00000389138.7:n.944C=
NM_005236.2:c.1667C= , LRG_463t1:c.1667C=	NP_005227.1:p.Pro556=
XM_011522424.1:c.1805C=	XP_011520726.1:p.Pro602=
XM_011522425.1:c.1124C=	XP_011520727.1:p.Pro375=
XM_011522426.1:c.878C=	XP_011520728.1:p.Pro293=
XM_011522427.1:c.317C=	XP_011520729.1:p.Pro106=
XR_932805.1:n.1826C=
XM_011522424.3:c.1805C=	XP_011520726.1:p.Pro602=
XM_017023043.2:c.878C=	XP_016878532.1:p.Pro293=
NM_005236.3:c.1667C= MANE Select	NP_005227.1:p.Pro556=