Canonical Allele Identifier: CA1627387717
Gene: MMUT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49447928_49447929delinsTC , CM000668.2:g.49447928_49447929delinsTC GRCh38
NC_000006.11:g.49415641_49415642delinsTC , CM000668.1:g.49415641_49415642delinsTC GRCh37
NC_000006.10:g.49523600_49523601delinsTC NCBI36
NG_007100.1:g.20211_20212delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.1445-144_1445-143delinsGA MANE Select ENSP00000274813.3:n.1445-144_1445-143delinsGA
ENST00000274813.3:c.1445-144_1445-143delinsGA ENSP00000274813.3:n.1445-144_1445-143delinsGA
NM_000255.3:c.1445-144_1445-143delinsGA NP_000246.2:n.1445-144_1445-143delinsGA
XM_005249143.2:c.1445-144_1445-143delinsGA XP_005249200.1:n.1445-144_1445-143delinsGA
XM_005249143.3:c.1445-144_1445-143delinsGA XP_005249200.1:n.1445-144_1445-143delinsGA
NM_000255.4:c.1445-144_1445-143delinsGA MANE Select NP_000246.2:n.1445-144_1445-143delinsGA