Canonical Allele Identifier: CA322870717
Gene: MN1 HGNC NCBI

Linked Data

dbSNP Id: rs942746927

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750874del , CM000684.2:g.27750874del GRCh38
NC_000022.10:g.28146862del , CM000684.1:g.28146862del GRCh37
NC_000022.9:g.26476862del NCBI36
NG_023258.1:g.55629del

Transcript Alleles

HGVS Amino-acid Change
ENST00000703102.1:n.533del
ENST00000302326.5:c.*45del MANE Select ENSP00000304956.4:n.*45del
ENST00000302326.4:c.*45del ENSP00000304956.4:n.*45del
ENST00000424656.1:c.361del
ENST00000497225.1:n.364del
NM_002430.2:c.*45del NP_002421.3:n.*45del
NM_002430.3:c.*45del MANE Select NP_002421.3:n.*45del