Canonical Allele Identifier: CA1627388066
Gene: MMUT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49448750C= , CM000668.2:g.49448750C= GRCh38
NC_000006.11:g.49416463C= , CM000668.1:g.49416463C= GRCh37
NC_000006.10:g.49524422C= NCBI36
NG_007100.1:g.19390G=

Transcript Alleles

HGVS Amino-acid change
ENST00000274813.4:c.1444+66G= MANE Select ENSP00000274813.3:n.1444+66G=
ENST00000274813.3:c.1444+66G= ENSP00000274813.3:n.1444+66G=
NM_000255.3:c.1444+66G= NP_000246.2:n.1444+66G=
XM_005249143.2:c.1444+66G= XP_005249200.1:n.1444+66G=
XM_005249143.3:c.1444+66G= XP_005249200.1:n.1444+66G=
NM_000255.4:c.1444+66G= MANE Select NP_000246.2:n.1444+66G=
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