Canonical Allele Identifier: CA2399818093
Gene: MN1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750908T= , CM000684.2:g.27750908T= GRCh38
NC_000022.10:g.28146896T= , CM000684.1:g.28146896T= GRCh37
NC_000022.9:g.26476896T= NCBI36
NG_023258.1:g.55591A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000703102.1:n.495A=
ENST00000302326.5:c.*7A= MANE Select ENSP00000304956.4:n.*7A=
ENST00000302326.4:c.*7A= ENSP00000304956.4:n.*7A=
ENST00000424656.1:c.323A=
ENST00000497225.1:n.326A=
NM_002430.2:c.*7A= NP_002421.3:n.*7A=
NM_002430.3:c.*7A= MANE Select NP_002421.3:n.*7A=
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