Canonical Allele Identifier: CA1627395646
Gene: MMUT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49458086G= , CM000668.2:g.49458086G= GRCh38
NC_000006.11:g.49425799G= , CM000668.1:g.49425799G= GRCh37
NC_000006.10:g.49533758G= NCBI36
NG_007100.1:g.10054C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.386-28C= MANE Select ENSP00000274813.3:n.386-28C=
ENST00000274813.3:c.386-28C= ENSP00000274813.3:n.386-28C=
NM_000255.3:c.386-28C= NP_000246.2:n.386-28C=
XM_005249143.2:c.386-28C= XP_005249200.1:n.386-28C=
XM_005249143.3:c.386-28C= XP_005249200.1:n.386-28C=
NM_000255.4:c.386-28C= MANE Select NP_000246.2:n.386-28C=
Search 100 bp 5'
Search 100 bp 3'