Canonical Allele Identifier: CA1627396905
Gene: MMUT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49459262_49459264delinsTAG , CM000668.2:g.49459262_49459264delinsTAG GRCh38
NC_000006.11:g.49426975_49426977delinsTAG , CM000668.1:g.49426975_49426977delinsTAG GRCh37
NC_000006.10:g.49534934_49534936delinsTAG NCBI36
NG_007100.1:g.8876_8878delinsCTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.203_205delinsCTA MANE Select ENSP00000274813.3:p.Ser68=
ENST00000274813.3:c.203_205delinsCTA ENSP00000274813.3:p.Ser68=
NM_000255.3:c.203_205delinsCTA NP_000246.2:p.Ser68=
XM_005249143.2:c.203_205delinsCTA XP_005249200.1:p.Ser68=
XM_005249143.3:c.203_205delinsCTA XP_005249200.1:p.Ser68=
NM_000255.4:c.203_205delinsCTA MANE Select NP_000246.2:p.Ser68=
Search 100 bp 5'
Search 100 bp 3'