Canonical Allele Identifier: CA1627395267
Gene: MMUT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49457839G= , CM000668.2:g.49457839G= GRCh38
NC_000006.11:g.49425552G= , CM000668.1:g.49425552G= GRCh37
NC_000006.10:g.49533511G= NCBI36
NG_007100.1:g.10301C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.605C= MANE Select ENSP00000274813.3:p.Thr202=
ENST00000274813.3:c.605C= ENSP00000274813.3:p.Thr202=
NM_000255.3:c.605C= NP_000246.2:p.Thr202=
XM_005249143.2:c.605C= XP_005249200.1:p.Thr202=
XM_005249143.3:c.605C= XP_005249200.1:p.Thr202=
NM_000255.4:c.605C= MANE Select NP_000246.2:p.Thr202=
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