Canonical Allele Identifier: CA2399817930
Gene: MN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750599A= , CM000684.2:g.27750599A= GRCh38
NC_000022.10:g.28146587A= , CM000684.1:g.28146587A= GRCh37
NC_000022.9:g.26476587A= NCBI36
NG_023258.1:g.55900T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000703102.1:n.804T=
ENST00000302326.5:c.*316T= MANE Select ENSP00000304956.4:n.*316T=
ENST00000302326.4:c.*316T= ENSP00000304956.4:n.*316T=
ENST00000424656.1:c.455+177T=
NM_002430.2:c.*316T= NP_002421.3:n.*316T=
NM_002430.3:c.*316T= MANE Select NP_002421.3:n.*316T=