Canonical Allele Identifier: CA2770993537
Gene: MMUT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49447990_49447993del , CM000668.2:g.49447990_49447993del GRCh38
NC_000006.11:g.49415703_49415706del , CM000668.1:g.49415703_49415706del GRCh37
NC_000006.10:g.49523662_49523665del NCBI36
NG_007100.1:g.20152_20155del

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.1445-203_1445-200del MANE Select ENSP00000274813.3:n.1445-203_1445-200del
ENST00000274813.3:c.1445-203_1445-200del ENSP00000274813.3:n.1445-203_1445-200del
NM_000255.3:c.1445-203_1445-200del NP_000246.2:n.1445-203_1445-200del
XM_005249143.2:c.1445-203_1445-200del XP_005249200.1:n.1445-203_1445-200del
XM_005249143.3:c.1445-203_1445-200del XP_005249200.1:n.1445-203_1445-200del
NM_000255.4:c.1445-203_1445-200del MANE Select NP_000246.2:n.1445-203_1445-200del