Canonical Allele Identifier: CA567155994
Gene: MMUT HGNC NCBI

Linked Data

dbSNP Id: rs1236825543
gnomAD v2: 6-49427207-A-AT
gnomAD v3: 6-49459494-A-AT
gnomAD v4: 6-49459494-A-AT
MyVariant Identifiers: chr6:g.49427207_49427208insT (hg19) chr6:g.49459494_49459495insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49459495dup , CM000668.2:g.49459495dup GRCh38
NC_000006.11:g.49427208dup , CM000668.1:g.49427208dup GRCh37
NC_000006.10:g.49535167dup NCBI36
NG_007100.1:g.8645dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.-29dup MANE Select ENSP00000274813.3:n.-29dup
ENST00000274813.3:c.-29dup ENSP00000274813.3:n.-29dup
NM_000255.3:c.-29dup NP_000246.2:n.-29dup
XM_005249143.2:c.-29dup XP_005249200.1:n.-29dup
XM_005249143.3:c.-29dup XP_005249200.1:n.-29dup
NM_000255.4:c.-29dup MANE Select NP_000246.2:n.-29dup
Search 100 bp 5'
Search 100 bp 3'