Canonical Allele Identifier: CA658094780
Gene: MN1 HGNC NCBI

Linked Data

COSMIC: COSN16131175
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750832_27750833insC , CM000684.2:g.27750832_27750833insC GRCh38
NC_000022.10:g.28146820_28146821insC , CM000684.1:g.28146820_28146821insC GRCh37
NC_000022.9:g.26476820_26476821insC NCBI36
NG_023258.1:g.55666_55667insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000703102.1:n.570_571insG
ENST00000302326.5:c.*82_*83insG MANE Select ENSP00000304956.4:n.*82_*83insG
ENST00000302326.4:c.*82_*83insG ENSP00000304956.4:n.*82_*83insG
ENST00000424656.1:c.398_399insG
ENST00000497225.1:n.401_402insG
NM_002430.2:c.*82_*83insG NP_002421.3:n.*82_*83insG
NM_002430.3:c.*82_*83insG MANE Select NP_002421.3:n.*82_*83insG
Search 100 bp 5'
Search 100 bp 3'