Canonical Allele Identifier: CA2209081403

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13944736A= , CM000678.2:g.13944736A=	GRCh38
NC_000016.9:g.14038593A= , CM000678.1:g.14038593A=	GRCh37
NC_000016.8:g.13946094A=	NCBI36
NG_011442.1:g.29580A= , LRG_463:g.29580A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2056A=	ENSP00000507912.1:p.Met686=
ENST00000683962.1:c.*1612A=	ENSP00000506854.1:n.*1612A=
ENST00000311895.8:c.1918A= MANE Select	ENSP00000310520.7:p.Met640=
ENST00000311895.7:c.1918A=	ENSP00000310520.7:p.Met640=
ENST00000389138.7:n.1195A=
ENST00000462862.1:c.231A=	ENSP00000461322.1:n.231A=
NM_005236.2:c.1918A= , LRG_463t1:c.1918A=	NP_005227.1:p.Met640=
XM_011522424.1:c.2056A=	XP_011520726.1:p.Met686=
XM_011522425.1:c.1375A=	XP_011520727.1:p.Met459=
XM_011522426.1:c.1129A=	XP_011520728.1:p.Met377=
XM_011522427.1:c.568A=	XP_011520729.1:p.Met190=
XR_932805.1:n.2077A=
XM_011522424.3:c.2056A=	XP_011520726.1:p.Met686=
XM_017023043.2:c.1129A=	XP_016878532.1:p.Met377=
NM_005236.3:c.1918A= MANE Select	NP_005227.1:p.Met640=