Canonical Allele Identifier: CA3265657893
Community Standard Title: NM_005236.3(ERCC4):c.2304_2376del (p.Leu769PhefsTer24)
Gene: ERCC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.13947900_13947972del , CM000678.2:g.13947900_13947972del GRCh38
NC_000016.9:g.14041757_14041829del , CM000678.1:g.14041757_14041829del GRCh37
NC_000016.8:g.13949258_13949330del NCBI36
NG_011442.1:g.32744_32816del , LRG_463:g.32744_32816del

Transcript Alleles

HGVS Amino-acid Change
NM_005236.3:c.2304_2376del MANE Select NP_005227.1:p.Leu769PhefsTer24
ENST00000311895.8:c.2304_2376del MANE Select ENSP00000310520.7:p.Leu769PhefsTer24
NM_005236.2:c.2304_2376del , LRG_463t1:c.2304_2376del NP_005227.1:p.Leu769PhefsTer24
ENST00000311895.7:c.2304_2376del ENSP00000310520.7:p.Leu769PhefsTer24
ENST00000389138.7:n.1581_1653del
ENST00000462862.1:c.617_689del ENSP00000461322.1:n.617_689del
ENST00000682617.1:c.2442_2514del ENSP00000507912.1:p.Leu815PhefsTer24
ENST00000683962.1:c.*1998_*2070del ENSP00000506854.1:n.*1998_*2070del
XM_011522424.1:c.2442_2514del XP_011520726.1:p.Leu815PhefsTer24
XM_011522424.3:c.2442_2514del XP_011520726.1:p.Leu815PhefsTer24
XM_011522425.1:c.1761_1833del XP_011520727.1:p.Leu588PhefsTer24
XM_011522426.1:c.1515_1587del XP_011520728.1:p.Leu506PhefsTer24
XM_011522427.1:c.954_1026del XP_011520729.1:p.Leu319PhefsTer24
XM_017023043.2:c.1515_1587del XP_016878532.1:p.Leu506PhefsTer24
XR_932805.1:n.2463_2535del