Canonical Allele Identifier: CA1627395685
Gene: MMUT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49458144_49458155delinsGATTCATCTCAT , CM000668.2:g.49458144_49458155delinsGATTCATCTCAT GRCh38
NC_000006.11:g.49425857_49425868delinsGATTCATCTCAT , CM000668.1:g.49425857_49425868delinsGATTCATCTCAT GRCh37
NC_000006.10:g.49533816_49533827delinsGATTCATCTCAT NCBI36
NG_007100.1:g.9985_9996delinsATGAGATGAATC

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.386-97_386-86delinsATGAGATGAATC MANE Select ENSP00000274813.3:n.386-97_386-86delinsATGAGATGAATC
ENST00000274813.3:c.386-97_386-86delinsATGAGATGAATC ENSP00000274813.3:n.386-97_386-86delinsATGAGATGAATC
NM_000255.3:c.386-97_386-86delinsATGAGATGAATC NP_000246.2:n.386-97_386-86delinsATGAGATGAATC
XM_005249143.2:c.386-97_386-86delinsATGAGATGAATC XP_005249200.1:n.386-97_386-86delinsATGAGATGAATC
XM_005249143.3:c.386-97_386-86delinsATGAGATGAATC XP_005249200.1:n.386-97_386-86delinsATGAGATGAATC
NM_000255.4:c.386-97_386-86delinsATGAGATGAATC MANE Select NP_000246.2:n.386-97_386-86delinsATGAGATGAATC