Canonical Allele Identifier: CA2770993608
Gene: MMUT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49459486del , CM000668.2:g.49459486del GRCh38
NC_000006.11:g.49427199del , CM000668.1:g.49427199del GRCh37
NC_000006.10:g.49535158del NCBI36
NG_007100.1:g.8656del

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.-18del MANE Select ENSP00000274813.3:n.-18del
ENST00000274813.3:c.-18del ENSP00000274813.3:n.-18del
NM_000255.3:c.-18del NP_000246.2:n.-18del
XM_005249143.2:c.-18del XP_005249200.1:n.-18del
XM_005249143.3:c.-18del XP_005249200.1:n.-18del
NM_000255.4:c.-18del MANE Select NP_000246.2:n.-18del