Canonical Allele Identifier: CA2209082821
Gene: ERCC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.13948009_13948012delinsTCTC , CM000678.2:g.13948009_13948012delinsTCTC GRCh38
NC_000016.9:g.14041866_14041869delinsTCTC , CM000678.1:g.14041866_14041869delinsTCTC GRCh37
NC_000016.8:g.13949367_13949370delinsTCTC NCBI36
NG_011442.1:g.32853_32856delinsTCTC , LRG_463:g.32853_32856delinsTCTC

Transcript Alleles

HGVS Amino-acid change
ENST00000682617.1:c.2551_2554delinsTCTC ENSP00000507912.1:p.Ser851=
ENST00000683962.1:c.*2107_*2110delinsTCTC ENSP00000506854.1:n.*2107_*2110delinsTCTC...
ENST00000311895.8:c.2413_2416delinsTCTC MANE Select ENSP00000310520.7:p.Ser805=
ENST00000311895.7:c.2413_2416delinsTCTC ENSP00000310520.7:p.Ser805=
ENST00000389138.7:n.1690_1693delinsTCTC
NM_005236.2:c.2413_2416delinsTCTC , LRG_463t1:c.2413_2416delinsTCTC NP_005227.1:p.Ser805=
XM_011522424.1:c.2551_2554delinsTCTC XP_011520726.1:p.Ser851=
XM_011522425.1:c.1870_1873delinsTCTC XP_011520727.1:p.Ser624=
XM_011522426.1:c.1624_1627delinsTCTC XP_011520728.1:p.Ser542=
XM_011522427.1:c.1063_1066delinsTCTC XP_011520729.1:p.Ser355=
XR_932805.1:n.2572_2575delinsTCTC
XM_011522424.3:c.2551_2554delinsTCTC XP_011520726.1:p.Ser851=
XM_017023043.2:c.1624_1627delinsTCTC XP_016878532.1:p.Ser542=
NM_005236.3:c.2413_2416delinsTCTC MANE Select NP_005227.1:p.Ser805=