Canonical Allele Identifier: CA2655934377
Gene: MN1 HGNC NCBI

Linked Data

gnomAD v4: 22-27750607-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750607A>T , CM000684.2:g.27750607A>T GRCh38
NC_000022.10:g.28146595A>T , CM000684.1:g.28146595A>T GRCh37
NC_000022.9:g.26476595A>T NCBI36
NG_023258.1:g.55892T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000703102.1:n.796T>A
ENST00000302326.5:c.*308T>A MANE Select ENSP00000304956.4:n.*308T>A
ENST00000302326.4:c.*308T>A ENSP00000304956.4:n.*308T>A
ENST00000424656.1:c.455+169T>A
NM_002430.2:c.*308T>A NP_002421.3:n.*308T>A
NM_002430.3:c.*308T>A MANE Select NP_002421.3:n.*308T>A
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