Canonical Allele Identifier: CA2679046447
Gene: MMUT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49447867_49447868del , CM000668.2:g.49447867_49447868del GRCh38
NC_000006.11:g.49415580_49415581del , CM000668.1:g.49415580_49415581del GRCh37
NC_000006.10:g.49523539_49523540del NCBI36
NG_007100.1:g.20273_20274del

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.1445-82_1445-81del MANE Select ENSP00000274813.3:n.1445-82_1445-81del
ENST00000274813.3:c.1445-82_1445-81del ENSP00000274813.3:n.1445-82_1445-81del
NM_000255.3:c.1445-82_1445-81del NP_000246.2:n.1445-82_1445-81del
XM_005249143.2:c.1445-82_1445-81del XP_005249200.1:n.1445-82_1445-81del
XM_005249143.3:c.1445-82_1445-81del XP_005249200.1:n.1445-82_1445-81del
NM_000255.4:c.1445-82_1445-81del MANE Select NP_000246.2:n.1445-82_1445-81del