Canonical Allele Identifier: CA752089817
Gene: MN1 HGNC NCBI

Linked Data

dbSNP Id: rs1351990942
MyVariant Identifiers: chr22:g.28146429del (hg19) chr22:g.27750441del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750441del , CM000684.2:g.27750441del GRCh38
NC_000022.10:g.28146429del , CM000684.1:g.28146429del GRCh37
NC_000022.9:g.26476429del NCBI36
NG_023258.1:g.56058del

Transcript Alleles

HGVS Amino-acid Change
ENST00000703102.1:n.962del
ENST00000302326.5:c.*474del MANE Select ENSP00000304956.4:n.*474del
ENST00000302326.4:c.*474del ENSP00000304956.4:n.*474del
ENST00000424656.1:c.456-213del
NM_002430.2:c.*474del NP_002421.3:n.*474del
NM_002430.3:c.*474del MANE Select NP_002421.3:n.*474del
Search 100 bp 5'
Search 100 bp 3'