Canonical Allele Identifier: CA2577674653
Gene: MN1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750841G>T , CM000684.2:g.27750841G>T GRCh38
NC_000022.10:g.28146829G>T , CM000684.1:g.28146829G>T GRCh37
NC_000022.9:g.26476829G>T NCBI36
NG_023258.1:g.55658C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000703102.1:n.562C>A
ENST00000302326.5:c.*74C>A MANE Select ENSP00000304956.4:n.*74C>A
ENST00000302326.4:c.*74C>A ENSP00000304956.4:n.*74C>A
ENST00000424656.1:c.390C>A
ENST00000497225.1:n.393C>A
NM_002430.2:c.*74C>A NP_002421.3:n.*74C>A
NM_002430.3:c.*74C>A MANE Select NP_002421.3:n.*74C>A
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