Canonical Allele Identifier: CA3218936100

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13947950G= , CM000678.2:g.13947950G=	GRCh38
NC_000016.9:g.14041807G= , CM000678.1:g.14041807G=	GRCh37
NC_000016.8:g.13949308G=	NCBI36
NG_011442.1:g.32794G= , LRG_463:g.32794G=

Transcript Alleles

HGVS	Amino-acid Change
NM_005236.3:c.2354G= MANE Select	NP_005227.1:p.Ser785=
ENST00000311895.8:c.2354G= MANE Select	ENSP00000310520.7:p.Ser785=
NM_005236.2:c.2354G= , LRG_463t1:c.2354G=	NP_005227.1:p.Ser785=
ENST00000311895.7:c.2354G=	ENSP00000310520.7:p.Ser785=
ENST00000389138.7:n.1631G=
ENST00000462862.1:c.667G=	ENSP00000461322.1:n.667G=
ENST00000682617.1:c.2492G=	ENSP00000507912.1:p.Ser831=
ENST00000683962.1:c.*2048G=	ENSP00000506854.1:n.*2048G=
XM_011522424.1:c.2492G=	XP_011520726.1:p.Ser831=
XM_011522424.3:c.2492G=	XP_011520726.1:p.Ser831=
XM_011522425.1:c.1811G=	XP_011520727.1:p.Ser604=
XM_011522426.1:c.1565G=	XP_011520728.1:p.Ser522=
XM_011522427.1:c.1004G=	XP_011520729.1:p.Ser335=
XM_017023043.2:c.1565G=	XP_016878532.1:p.Ser522=
XR_932805.1:n.2513G=