Canonical Allele Identifier: CA2679046430
Gene: MMUT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49447830_49447831del , CM000668.2:g.49447830_49447831del GRCh38
NC_000006.11:g.49415543_49415544del , CM000668.1:g.49415543_49415544del GRCh37
NC_000006.10:g.49523502_49523503del NCBI36
NG_007100.1:g.20309_20310del

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.1445-46_1445-45del MANE Select ENSP00000274813.3:n.1445-46_1445-45del
ENST00000274813.3:c.1445-46_1445-45del ENSP00000274813.3:n.1445-46_1445-45del
NM_000255.3:c.1445-46_1445-45del NP_000246.2:n.1445-46_1445-45del
XM_005249143.2:c.1445-46_1445-45del XP_005249200.1:n.1445-46_1445-45del
XM_005249143.3:c.1445-46_1445-45del XP_005249200.1:n.1445-46_1445-45del
NM_000255.4:c.1445-46_1445-45del MANE Select NP_000246.2:n.1445-46_1445-45del