Canonical Allele Identifier: CA2655934368
Gene: MN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750584del , CM000684.2:g.27750584del GRCh38
NC_000022.10:g.28146572del , CM000684.1:g.28146572del GRCh37
NC_000022.9:g.26476572del NCBI36
NG_023258.1:g.55920del

Transcript Alleles

HGVS Amino-acid Change
ENST00000703102.1:n.824del
ENST00000302326.5:c.*336del MANE Select ENSP00000304956.4:n.*336del
ENST00000302326.4:c.*336del ENSP00000304956.4:n.*336del
ENST00000424656.1:c.455+197del
NM_002430.2:c.*336del NP_002421.3:n.*336del
NM_002430.3:c.*336del MANE Select NP_002421.3:n.*336del