Canonical Allele Identifier: CA1627386272
Gene: MMUT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49444515G= , CM000668.2:g.49444515G= GRCh38
NC_000006.11:g.49412228G= , CM000668.1:g.49412228G= GRCh37
NC_000006.10:g.49520187G= NCBI36
NG_007100.1:g.23625C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.1676+124C= MANE Select ENSP00000274813.3:n.1676+124C=
ENST00000274813.3:c.1676+124C= ENSP00000274813.3:n.1676+124C=
NM_000255.3:c.1676+124C= NP_000246.2:n.1676+124C=
XM_005249143.2:c.1676+124C= XP_005249200.1:n.1676+124C=
XM_005249143.3:c.1676+124C= XP_005249200.1:n.1676+124C=
NM_000255.4:c.1676+124C= MANE Select NP_000246.2:n.1676+124C=
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