Canonical Allele Identifier: CA2399818023
Gene: MN1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750798T= , CM000684.2:g.27750798T= GRCh38
NC_000022.10:g.28146786T= , CM000684.1:g.28146786T= GRCh37
NC_000022.9:g.26476786T= NCBI36
NG_023258.1:g.55701A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000703102.1:n.605A=
ENST00000302326.5:c.*117A= MANE Select ENSP00000304956.4:n.*117A=
ENST00000302326.4:c.*117A= ENSP00000304956.4:n.*117A=
ENST00000424656.1:c.433A=
ENST00000497225.1:n.436A=
NM_002430.2:c.*117A= NP_002421.3:n.*117A=
NM_002430.3:c.*117A= MANE Select NP_002421.3:n.*117A=
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