Canonical Allele Identifier: CA2209082842
Gene: ERCC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.13948047A= , CM000678.2:g.13948047A= GRCh38
NC_000016.9:g.14041904A= , CM000678.1:g.14041904A= GRCh37
NC_000016.8:g.13949405A= NCBI36
NG_011442.1:g.32891A= , LRG_463:g.32891A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682617.1:c.2589A= ENSP00000507912.1:p.Lys863=
ENST00000683962.1:c.*2145A= ENSP00000506854.1:n.*2145A=
ENST00000311895.8:c.2451A= MANE Select ENSP00000310520.7:p.Lys817=
ENST00000311895.7:c.2451A= ENSP00000310520.7:p.Lys817=
ENST00000389138.7:n.1728A=
NM_005236.2:c.2451A= , LRG_463t1:c.2451A= NP_005227.1:p.Lys817=
XM_011522424.1:c.2589A= XP_011520726.1:p.Lys863=
XM_011522425.1:c.1908A= XP_011520727.1:p.Lys636=
XM_011522426.1:c.1662A= XP_011520728.1:p.Lys554=
XM_011522427.1:c.1101A= XP_011520729.1:p.Lys367=
XR_932805.1:n.2610A=
XM_011522424.3:c.2589A= XP_011520726.1:p.Lys863=
XM_017023043.2:c.1662A= XP_016878532.1:p.Lys554=
NM_005236.3:c.2451A= MANE Select NP_005227.1:p.Lys817=