Canonical Allele Identifier: CA2841020026
Gene: MMUT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49458024dup , CM000668.2:g.49458024dup GRCh38
NC_000006.11:g.49425737dup , CM000668.1:g.49425737dup GRCh37
NC_000006.10:g.49533696dup NCBI36
NG_007100.1:g.10117dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.421dup MANE Select ENSP00000274813.3:p.Ala141GlyfsTer7
ENST00000274813.3:c.421dup ENSP00000274813.3:p.Ala141GlyfsTer7
NM_000255.3:c.421dup NP_000246.2:p.Ala141GlyfsTer7
XM_005249143.2:c.421dup XP_005249200.1:p.Ala141GlyfsTer7
XM_005249143.3:c.421dup XP_005249200.1:p.Ala141GlyfsTer7
NM_000255.4:c.421dup MANE Select NP_000246.2:p.Ala141GlyfsTer7
Search 100 bp 5'
Search 100 bp 3'