Canonical Allele Identifier: CA1627396760
Gene: MMUT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49459205C= , CM000668.2:g.49459205C= GRCh38
NC_000006.11:g.49426918C= , CM000668.1:g.49426918C= GRCh37
NC_000006.10:g.49534877C= NCBI36
NG_007100.1:g.8935G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.262G= MANE Select ENSP00000274813.3:p.Val88=
ENST00000274813.3:c.262G= ENSP00000274813.3:p.Val88=
NM_000255.3:c.262G= NP_000246.2:p.Val88=
XM_005249143.2:c.262G= XP_005249200.1:p.Val88=
XM_005249143.3:c.262G= XP_005249200.1:p.Val88=
NM_000255.4:c.262G= MANE Select NP_000246.2:p.Val88=
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