Canonical Allele Identifier: CA2399818078
Gene: MN1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750892G= , CM000684.2:g.27750892G= GRCh38
NC_000022.10:g.28146880G= , CM000684.1:g.28146880G= GRCh37
NC_000022.9:g.26476880G= NCBI36
NG_023258.1:g.55607C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000703102.1:n.511C=
ENST00000302326.5:c.*23C= MANE Select ENSP00000304956.4:n.*23C=
ENST00000302326.4:c.*23C= ENSP00000304956.4:n.*23C=
ENST00000424656.1:c.339C=
ENST00000497225.1:n.342C=
NM_002430.2:c.*23C= NP_002421.3:n.*23C=
NM_002430.3:c.*23C= MANE Select NP_002421.3:n.*23C=
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