Canonical Allele Identifier: CA1627396769
Gene: MMUT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49459207C= , CM000668.2:g.49459207C= GRCh38
NC_000006.11:g.49426920C= , CM000668.1:g.49426920C= GRCh37
NC_000006.10:g.49534879C= NCBI36
NG_007100.1:g.8933G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.260G= MANE Select ENSP00000274813.3:p.Gly87=
ENST00000274813.3:c.260G= ENSP00000274813.3:p.Gly87=
NM_000255.3:c.260G= NP_000246.2:p.Gly87=
XM_005249143.2:c.260G= XP_005249200.1:p.Gly87=
XM_005249143.3:c.260G= XP_005249200.1:p.Gly87=
NM_000255.4:c.260G= MANE Select NP_000246.2:p.Gly87=
Search 100 bp 5'
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