Canonical Allele Identifier: CA2528717183
Gene: MMUT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49458120_49458124del , CM000668.2:g.49458120_49458124del GRCh38
NC_000006.11:g.49425833_49425837del , CM000668.1:g.49425833_49425837del GRCh37
NC_000006.10:g.49533792_49533796del NCBI36
NG_007100.1:g.10019_10023del

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.386-63_386-59del MANE Select ENSP00000274813.3:n.386-63_386-59del
ENST00000274813.3:c.386-63_386-59del ENSP00000274813.3:n.386-63_386-59del
NM_000255.3:c.386-63_386-59del NP_000246.2:n.386-63_386-59del
XM_005249143.2:c.386-63_386-59del XP_005249200.1:n.386-63_386-59del
XM_005249143.3:c.386-63_386-59del XP_005249200.1:n.386-63_386-59del
NM_000255.4:c.386-63_386-59del MANE Select NP_000246.2:n.386-63_386-59del