Canonical Allele Identifier: CA8908097
Gene: MIB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.21779448del , CM000680.2:g.21779448del GRCh38
NC_000018.9:g.19359409del , CM000680.1:g.19359409del GRCh37
NC_000018.8:g.17613407del NCBI36
NG_033272.2:g.79492del , LRG_759:g.79492del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261537.7:c.704-33del MANE Select ENSP00000261537.6:n.704-33del
ENST00000261537.6:c.704-33del ENSP00000261537.6:n.704-33del
ENST00000578646.5:n.642-33del
NM_020774.3:c.704-33del , LRG_759t1:c.704-33del NP_065825.1:n.704-33del
XR_935234.1:n.1495-33del
XR_935235.1:n.1495-33del
XM_017025873.1:c.188-33del XP_016881362.1:n.188-33del
XM_017025874.1:c.704-33del XP_016881363.1:n.704-33del
XM_017025875.1:c.704-33del XP_016881364.1:n.704-33del
NM_020774.4:c.704-33del MANE Select NP_065825.1:n.704-33del