Canonical Allele Identifier: CA1627386300
Gene: MMUT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49444617C= , CM000668.2:g.49444617C= GRCh38
NC_000006.11:g.49412330C= , CM000668.1:g.49412330C= GRCh37
NC_000006.10:g.49520289C= NCBI36
NG_007100.1:g.23523G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.1676+22G= MANE Select ENSP00000274813.3:n.1676+22G=
ENST00000274813.3:c.1676+22G= ENSP00000274813.3:n.1676+22G=
NM_000255.3:c.1676+22G= NP_000246.2:n.1676+22G=
XM_005249143.2:c.1676+22G= XP_005249200.1:n.1676+22G=
XM_005249143.3:c.1676+22G= XP_005249200.1:n.1676+22G=
NM_000255.4:c.1676+22G= MANE Select NP_000246.2:n.1676+22G=
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