Canonical Allele Identifier: CA2209081410

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13944745C= , CM000678.2:g.13944745C=	GRCh38
NC_000016.9:g.14038602C= , CM000678.1:g.14038602C=	GRCh37
NC_000016.8:g.13946103C=	NCBI36
NG_011442.1:g.29589C= , LRG_463:g.29589C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2065C=	ENSP00000507912.1:p.Pro689=
ENST00000683962.1:c.*1621C=	ENSP00000506854.1:n.*1621C=
ENST00000311895.8:c.1927C= MANE Select	ENSP00000310520.7:p.Pro643=
ENST00000311895.7:c.1927C=	ENSP00000310520.7:p.Pro643=
ENST00000389138.7:n.1204C=
ENST00000462862.1:c.240C=	ENSP00000461322.1:n.240C=
NM_005236.2:c.1927C= , LRG_463t1:c.1927C=	NP_005227.1:p.Pro643=
XM_011522424.1:c.2065C=	XP_011520726.1:p.Pro689=
XM_011522425.1:c.1384C=	XP_011520727.1:p.Pro462=
XM_011522426.1:c.1138C=	XP_011520728.1:p.Pro380=
XM_011522427.1:c.577C=	XP_011520729.1:p.Pro193=
XR_932805.1:n.2086C=
XM_011522424.3:c.2065C=	XP_011520726.1:p.Pro689=
XM_017023043.2:c.1138C=	XP_016878532.1:p.Pro380=
NM_005236.3:c.1927C= MANE Select	NP_005227.1:p.Pro643=