Canonical Allele Identifier: CA2679046427
Gene: MMUT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49447827_49447828del , CM000668.2:g.49447827_49447828del GRCh38
NC_000006.11:g.49415540_49415541del , CM000668.1:g.49415540_49415541del GRCh37
NC_000006.10:g.49523499_49523500del NCBI36
NG_007100.1:g.20312_20313del

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.1445-43_1445-42del MANE Select ENSP00000274813.3:n.1445-43_1445-42del
ENST00000274813.3:c.1445-43_1445-42del ENSP00000274813.3:n.1445-43_1445-42del
NM_000255.3:c.1445-43_1445-42del NP_000246.2:n.1445-43_1445-42del
XM_005249143.2:c.1445-43_1445-42del XP_005249200.1:n.1445-43_1445-42del
XM_005249143.3:c.1445-43_1445-42del XP_005249200.1:n.1445-43_1445-42del
NM_000255.4:c.1445-43_1445-42del MANE Select NP_000246.2:n.1445-43_1445-42del