Canonical Allele Identifier: CA1627396559
Gene: MMUT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49459137A= , CM000668.2:g.49459137A= GRCh38
NC_000006.11:g.49426850A= , CM000668.1:g.49426850A= GRCh37
NC_000006.10:g.49534809A= NCBI36
NG_007100.1:g.9003T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.330T= MANE Select ENSP00000274813.3:p.Tyr110=
ENST00000274813.3:c.330T= ENSP00000274813.3:p.Tyr110=
NM_000255.3:c.330T= NP_000246.2:p.Tyr110=
XM_005249143.2:c.330T= XP_005249200.1:p.Tyr110=
XM_005249143.3:c.330T= XP_005249200.1:p.Tyr110=
NM_000255.4:c.330T= MANE Select NP_000246.2:p.Tyr110=
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