Canonical Allele Identifier: CA2399817886
Gene: MN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750510G= , CM000684.2:g.27750510G= GRCh38
NC_000022.10:g.28146498G= , CM000684.1:g.28146498G= GRCh37
NC_000022.9:g.26476498G= NCBI36
NG_023258.1:g.55989C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000703102.1:n.893C=
ENST00000302326.5:c.*405C= MANE Select ENSP00000304956.4:n.*405C=
ENST00000302326.4:c.*405C= ENSP00000304956.4:n.*405C=
ENST00000424656.1:c.455+266C=
NM_002430.2:c.*405C= NP_002421.3:n.*405C=
NM_002430.3:c.*405C= MANE Select NP_002421.3:n.*405C=