Canonical Allele Identifier: CA2209082881

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13948143A= , CM000678.2:g.13948143A=	GRCh38
NC_000016.9:g.14042000A= , CM000678.1:g.14042000A=	GRCh37
NC_000016.8:g.13949501A=	NCBI36
NG_011442.1:g.32987A= , LRG_463:g.32987A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682617.1:c.2685A=	ENSP00000507912.1:p.Gln895=
ENST00000683962.1:c.*2241A=	ENSP00000506854.1:n.*2241A=
ENST00000311895.8:c.2547A= MANE Select	ENSP00000310520.7:p.Gln849=
ENST00000311895.7:c.2547A=	ENSP00000310520.7:p.Gln849=
ENST00000389138.7:n.1824A=
NM_005236.2:c.2547A= , LRG_463t1:c.2547A=	NP_005227.1:p.Gln849=
XM_011522424.1:c.2685A=	XP_011520726.1:p.Gln895=
XM_011522425.1:c.2004A=	XP_011520727.1:p.Gln668=
XM_011522426.1:c.1758A=	XP_011520728.1:p.Gln586=
XM_011522427.1:c.1197A=	XP_011520729.1:p.Gln399=
XR_932805.1:n.2706A=
XM_011522424.3:c.2685A=	XP_011520726.1:p.Gln895=
XM_017023043.2:c.1758A=	XP_016878532.1:p.Gln586=
NM_005236.3:c.2547A= MANE Select	NP_005227.1:p.Gln849=