Canonical Allele Identifier: CA2209082910
Gene: ERCC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.13948196T= , CM000678.2:g.13948196T= GRCh38
NC_000016.9:g.14042053T= , CM000678.1:g.14042053T= GRCh37
NC_000016.8:g.13949554T= NCBI36
NG_011442.1:g.33040T= , LRG_463:g.33040T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682617.1:c.2738T= ENSP00000507912.1:p.Met913=
ENST00000683962.1:c.*2294T= ENSP00000506854.1:n.*2294T=
ENST00000311895.8:c.2600T= MANE Select ENSP00000310520.7:p.Met867=
ENST00000311895.7:c.2600T= ENSP00000310520.7:p.Met867=
ENST00000389138.7:n.1877T=
NM_005236.2:c.2600T= , LRG_463t1:c.2600T= NP_005227.1:p.Met867=
XM_011522424.1:c.2738T= XP_011520726.1:p.Met913=
XM_011522425.1:c.2057T= XP_011520727.1:p.Met686=
XM_011522426.1:c.1811T= XP_011520728.1:p.Met604=
XM_011522427.1:c.1250T= XP_011520729.1:p.Met417=
XR_932805.1:n.2759T=
XM_011522424.3:c.2738T= XP_011520726.1:p.Met913=
XM_017023043.2:c.1811T= XP_016878532.1:p.Met604=
NM_005236.3:c.2600T= MANE Select NP_005227.1:p.Met867=