Canonical Allele Identifier: CA2511671229
Gene: MMUT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49459169_49459170insAGG , CM000668.2:g.49459169_49459170insAGG GRCh38
NC_000006.11:g.49426882_49426883insAGG , CM000668.1:g.49426882_49426883insAGG GRCh37
NC_000006.10:g.49534841_49534842insAGG NCBI36
NG_007100.1:g.8970_8971insCCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.297_298insCCT MANE Select ENSP00000274813.3:p.Met99_Tyr100insPro
ENST00000274813.3:c.297_298insCCT ENSP00000274813.3:p.Met99_Tyr100insPro
NM_000255.3:c.297_298insCCT NP_000246.2:p.Met99_Tyr100insPro
XM_005249143.2:c.297_298insCCT XP_005249200.1:p.Met99_Tyr100insPro
XM_005249143.3:c.297_298insCCT XP_005249200.1:p.Met99_Tyr100insPro
NM_000255.4:c.297_298insCCT MANE Select NP_000246.2:p.Met99_Tyr100insPro
Search 100 bp 5'
Search 100 bp 3'