Canonical Allele Identifier: CA2805944182

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13948644G>T , CM000678.2:g.13948644G>T	GRCh38
NC_000016.9:g.14042501G>T , CM000678.1:g.14042501G>T	GRCh37
NC_000016.8:g.13950002G>T	NCBI36
NG_011442.1:g.33488G>T , LRG_463:g.33488G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.*297G>T	ENSP00000507912.1:n.*297G>T
ENST00000683962.1:c.*2742G>T	ENSP00000506854.1:n.*2742G>T
ENST00000311895.8:c.*297G>T MANE Select	ENSP00000310520.7:n.*297G>T
ENST00000311895.7:c.*297G>T	ENSP00000310520.7:n.*297G>T
NM_005236.2:c.*297G>T , LRG_463t1:c.*297G>T	NP_005227.1:n.*297G>T
XM_011522424.1:c.*297G>T	XP_011520726.1:n.*297G>T
XM_011522425.1:c.*297G>T	XP_011520727.1:n.*297G>T
XM_011522426.1:c.*297G>T	XP_011520728.1:n.*297G>T
XM_011522427.1:c.*297G>T	XP_011520729.1:n.*297G>T
XR_932805.1:n.3074-69G>T
XM_011522424.3:c.*297G>T	XP_011520726.1:n.*297G>T
XM_017023043.2:c.*297G>T	XP_016878532.1:n.*297G>T
NM_005236.3:c.*297G>T MANE Select	NP_005227.1:n.*297G>T