Canonical Allele Identifier: CA1627386273
Gene: MMUT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49444517T= , CM000668.2:g.49444517T= GRCh38
NC_000006.11:g.49412230T= , CM000668.1:g.49412230T= GRCh37
NC_000006.10:g.49520189T= NCBI36
NG_007100.1:g.23623A=

Transcript Alleles

HGVS Amino-acid change
ENST00000274813.4:c.1676+122A= MANE Select ENSP00000274813.3:n.1676+122A=
ENST00000274813.3:c.1676+122A= ENSP00000274813.3:n.1676+122A=
NM_000255.3:c.1676+122A= NP_000246.2:n.1676+122A=
XM_005249143.2:c.1676+122A= XP_005249200.1:n.1676+122A=
XM_005249143.3:c.1676+122A= XP_005249200.1:n.1676+122A=
NM_000255.4:c.1676+122A= MANE Select NP_000246.2:n.1676+122A=
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