Canonical Allele Identifier: CA2818640002
Gene: MN1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750457T>G , CM000684.2:g.27750457T>G GRCh38
NC_000022.10:g.28146445T>G , CM000684.1:g.28146445T>G GRCh37
NC_000022.9:g.26476445T>G NCBI36
NG_023258.1:g.56042A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000703102.1:n.946A>C
ENST00000302326.5:c.*458A>C MANE Select ENSP00000304956.4:n.*458A>C
ENST00000302326.4:c.*458A>C ENSP00000304956.4:n.*458A>C
ENST00000424656.1:c.456-229A>C
NM_002430.2:c.*458A>C NP_002421.3:n.*458A>C
NM_002430.3:c.*458A>C MANE Select NP_002421.3:n.*458A>C
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