Canonical Allele Identifier: CA1627397154
Gene: MMUT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49459405_49459406delinsTC , CM000668.2:g.49459405_49459406delinsTC GRCh38
NC_000006.11:g.49427118_49427119delinsTC , CM000668.1:g.49427118_49427119delinsTC GRCh37
NC_000006.10:g.49535077_49535078delinsTC NCBI36
NG_007100.1:g.8734_8735delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.61_62delinsGA MANE Select ENSP00000274813.3:p.Glu21=
ENST00000274813.3:c.61_62delinsGA ENSP00000274813.3:p.Glu21=
NM_000255.3:c.61_62delinsGA NP_000246.2:p.Glu21=
XM_005249143.2:c.61_62delinsGA XP_005249200.1:p.Glu21=
XM_005249143.3:c.61_62delinsGA XP_005249200.1:p.Glu21=
NM_000255.4:c.61_62delinsGA MANE Select NP_000246.2:p.Glu21=
Search 100 bp 5'
Search 100 bp 3'