Canonical Allele Identifier: CA513939213
Gene: MN1 HGNC NCBI

Linked Data

dbSNP Id: rs1555881002
gnomAD v2: 22-28146769-G-GGA
gnomAD v3: 22-27750781-G-GGA
gnomAD v4: 22-27750781-G-GGA
MyVariant Identifiers: chr22:g.28146769_28146770insGA (hg19) chr22:g.28146770delinsGAA (hg19) chr22:g.27750781_27750782insGA (hg38) chr22:g.27750782delinsGAA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750781_27750782insGA , CM000684.2:g.27750781_27750782insGA GRCh38
NC_000022.10:g.28146769_28146770insGA , CM000684.1:g.28146769_28146770insGA GRCh37
NC_000022.9:g.26476769_26476770insGA NCBI36
NG_023258.1:g.55717_55718insTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000703102.1:n.621_622insTC
ENST00000302326.5:c.*133_*134insTC MANE Select ENSP00000304956.4:n.*133_*134insTC
ENST00000302326.4:c.*133_*134insTC ENSP00000304956.4:n.*133_*134insTC
ENST00000424656.1:c.449_450insTC
ENST00000497225.1:n.452_453insTC
NM_002430.2:c.*133_*134insTC NP_002421.3:n.*133_*134insTC
NM_002430.3:c.*133_*134insTC MANE Select NP_002421.3:n.*133_*134insTC
Search 100 bp 5'
Search 100 bp 3'