Canonical Allele Identifier: CA1335778145
Gene: USP40 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233513310_233513314delinsACTTT , CM000664.2:g.233513310_233513314delinsACTTT GRCh38
NC_000002.11:g.234421956_234421960delinsACTTT , CM000664.1:g.234421956_234421960delinsACTTT GRCh37
NC_000002.10:g.234086695_234086699delinsACTTT NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000678225.2:c.2384-692_2384-688delinsAAAGT MANE Select ENSP00000502952.1:n.2384-692_2384-688deli...
ENST00000678225.1:c.2382-690_2382-686delinsAAAGT ENSP00000502952.1:n.2382-690_2382-686deli...
ENST00000251722.10:c.2381-692_2381-688delinsAAAGT ENSP00000251722.6:n.2381-692_2381-688deli...
ENST00000427112.6:c.2381-692_2381-688delinsAAAGT ENSP00000387898.2:n.2381-692_2381-688deli...
ENST00000450966.5:c.2417-692_2417-688delinsAAAGT ENSP00000415434.1:n.2417-692_2417-688deli...
NM_018218.2:c.2417-692_2417-688delinsAAAGT NP_060688.1:n.2417-692_2417-688delinsAAAG...
XM_006712612.2:c.2420-692_2420-688delinsAAAGT XP_006712675.1:n.2420-692_2420-688delinsA...
XM_011511396.1:c.2420-692_2420-688delinsAAAGT XP_011509698.1:n.2420-692_2420-688delinsA...
XM_011511397.1:c.2384-692_2384-688delinsAAAGT XP_011509699.1:n.2384-692_2384-688delinsA...
XM_011511398.1:c.2420-692_2420-688delinsAAAGT XP_011509700.1:n.2420-692_2420-688delinsA...
XM_011511399.1:c.2111-692_2111-688delinsAAAGT XP_011509701.1:n.2111-692_2111-688delinsA...
XM_011511400.1:c.2000-692_2000-688delinsAAAGT XP_011509702.1:n.2000-692_2000-688delinsA...
XM_011511401.1:c.2420-635_2420-631delinsAAAGT XP_011509703.1:n.2420-635_2420-631delinsA...
XM_011511402.1:c.866-692_866-688delinsAAAGT XP_011509704.1:n.866-692_866-688delinsAAA...
NM_001365479.1:c.2384-692_2384-688delinsAAAGT NP_001352408.1:n.2384-692_2384-688delinsA...
NM_018218.3:c.2381-692_2381-688delinsAAAGT NP_060688.2:n.2381-692_2381-688delinsAAAG...
XM_006712612.3:c.2420-692_2420-688delinsAAAGT XP_006712675.1:n.2420-692_2420-688delinsA...
XM_011511396.2:c.2420-692_2420-688delinsAAAGT XP_011509698.1:n.2420-692_2420-688delinsA...
XM_011511397.2:c.2384-692_2384-688delinsAAAGT XP_011509699.1:n.2384-692_2384-688delinsA...
XM_011511398.3:c.2420-692_2420-688delinsAAAGT XP_011509700.1:n.2420-692_2420-688delinsA...
XM_011511399.2:c.2111-692_2111-688delinsAAAGT XP_011509701.1:n.2111-692_2111-688delinsA...
XM_011511400.2:c.2000-692_2000-688delinsAAAGT XP_011509702.1:n.2000-692_2000-688delinsA...
XM_011511401.2:c.2420-635_2420-631delinsAAAGT XP_011509703.1:n.2420-635_2420-631delinsA...
XM_017004427.1:c.1349-692_1349-688delinsAAAGT XP_016859916.1:n.1349-692_1349-688delinsA...
XM_017004428.1:c.866-692_866-688delinsAAAGT XP_016859917.1:n.866-692_866-688delinsAAA...
XR_001738818.1:n.2435-692_2435-688delinsAAAGT
XR_001738819.1:n.2435-692_2435-688delinsAAAGT
XR_001738820.1:n.2509-692_2509-688delinsAAAGT
NM_001365479.2:c.2384-692_2384-688delinsAAAGT MANE Select NP_001352408.1:n.2384-692_2384-688delinsA...
NM_001382295.1:c.2384-692_2384-688delinsAAAGT NP_001369224.1:n.2384-692_2384-688delinsA...
NM_001382296.1:c.2384-692_2384-688delinsAAAGT NP_001369225.1:n.2384-692_2384-688delinsA...
NM_001382297.1:c.2384-692_2384-688delinsAAAGT NP_001369226.1:n.2384-692_2384-688delinsA...
NM_001382298.1:c.2111-692_2111-688delinsAAAGT NP_001369227.1:n.2111-692_2111-688delinsA...
NM_001382299.1:c.2228-692_2228-688delinsAAAGT NP_001369228.1:n.2228-692_2228-688delinsA...
NM_001382300.1:c.2384-692_2384-688delinsAAAGT NP_001369229.1:n.2384-692_2384-688delinsA...
NM_001382301.1:c.2384-692_2384-688delinsAAAGT NP_001369230.1:n.2384-692_2384-688delinsA...
NM_018218.4:c.2381-692_2381-688delinsAAAGT NP_060688.2:n.2381-692_2381-688delinsAAAG...
NR_168049.1:n.2570-692_2570-688delinsAAAGT
NR_168050.1:n.2568-692_2568-688delinsAAAGT
NR_168051.1:n.2502-692_2502-688delinsAAAGT
NR_168052.1:n.2502-692_2502-688delinsAAAGT
NR_168053.1:n.2511-692_2511-688delinsAAAGT
NR_168054.1:n.2323-692_2323-688delinsAAAGT