Canonical Allele Identifier: CA1627395667
Gene: MMUT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49458116_49458122delinsATTTACT , CM000668.2:g.49458116_49458122delinsATTTACT GRCh38
NC_000006.11:g.49425829_49425835delinsATTTACT , CM000668.1:g.49425829_49425835delinsATTTACT GRCh37
NC_000006.10:g.49533788_49533794delinsATTTACT NCBI36
NG_007100.1:g.10018_10024delinsAGTAAAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.386-64_386-58delinsAGTAAAT MANE Select ENSP00000274813.3:n.386-64_386-58delinsAGTAAAT
ENST00000274813.3:c.386-64_386-58delinsAGTAAAT ENSP00000274813.3:n.386-64_386-58delinsAGTAAAT
NM_000255.3:c.386-64_386-58delinsAGTAAAT NP_000246.2:n.386-64_386-58delinsAGTAAAT
XM_005249143.2:c.386-64_386-58delinsAGTAAAT XP_005249200.1:n.386-64_386-58delinsAGTAAAT
XM_005249143.3:c.386-64_386-58delinsAGTAAAT XP_005249200.1:n.386-64_386-58delinsAGTAAAT
NM_000255.4:c.386-64_386-58delinsAGTAAAT MANE Select NP_000246.2:n.386-64_386-58delinsAGTAAAT