Canonical Allele Identifier: CA2209083101
Gene: ERCC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.13948594T= , CM000678.2:g.13948594T= GRCh38
NC_000016.9:g.14042451T= , CM000678.1:g.14042451T= GRCh37
NC_000016.8:g.13949952T= NCBI36
NG_011442.1:g.33438T= , LRG_463:g.33438T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682617.1:c.*247T= ENSP00000507912.1:n.*247T=
ENST00000683962.1:c.*2692T= ENSP00000506854.1:n.*2692T=
ENST00000311895.8:c.*247T= MANE Select ENSP00000310520.7:n.*247T=
ENST00000311895.7:c.*247T= ENSP00000310520.7:n.*247T=
NM_005236.2:c.*247T= , LRG_463t1:c.*247T= NP_005227.1:n.*247T=
XM_011522424.1:c.*247T= XP_011520726.1:n.*247T=
XM_011522425.1:c.*247T= XP_011520727.1:n.*247T=
XM_011522426.1:c.*247T= XP_011520728.1:n.*247T=
XM_011522427.1:c.*247T= XP_011520729.1:n.*247T=
XR_932805.1:n.3073+84T=
XM_011522424.3:c.*247T= XP_011520726.1:n.*247T=
XM_017023043.2:c.*247T= XP_016878532.1:n.*247T=
NM_005236.3:c.*247T= MANE Select NP_005227.1:n.*247T=