Canonical Allele Identifier: CA2209081278

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13944426C= , CM000678.2:g.13944426C=	GRCh38
NC_000016.9:g.14038283C= , CM000678.1:g.14038283C=	GRCh37
NC_000016.8:g.13945784C=	NCBI36
NG_011442.1:g.29270C= , LRG_463:g.29270C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2043-297C=	ENSP00000507912.1:n.2043-297C=
ENST00000683962.1:c.*1599-297C=	ENSP00000506854.1:n.*1599-297C=
ENST00000311895.8:c.1905-297C= MANE Select	ENSP00000310520.7:n.1905-297C=
ENST00000311895.7:c.1905-297C=	ENSP00000310520.7:n.1905-297C=
ENST00000389138.7:n.1182-297C=
ENST00000462862.1:c.218-297C=	ENSP00000461322.1:n.218-297C=
NM_005236.2:c.1905-297C= , LRG_463t1:c.1905-297C=	NP_005227.1:n.1905-297C=
XM_011522424.1:c.2043-297C=	XP_011520726.1:n.2043-297C=
XM_011522425.1:c.1362-297C=	XP_011520727.1:n.1362-297C=
XM_011522426.1:c.1116-297C=	XP_011520728.1:n.1116-297C=
XM_011522427.1:c.555-297C=	XP_011520729.1:n.555-297C=
XR_932805.1:n.2064-297C=
XM_011522424.3:c.2043-297C=	XP_011520726.1:n.2043-297C=
XM_017023043.2:c.1116-297C=	XP_016878532.1:n.1116-297C=
NM_005236.3:c.1905-297C= MANE Select	NP_005227.1:n.1905-297C=