Canonical Allele Identifier: CA411032704
Gene: MN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750922A>T , CM000684.2:g.27750922A>T GRCh38
NC_000022.10:g.28146910A>T , CM000684.1:g.28146910A>T GRCh37
NC_000022.9:g.26476910A>T NCBI36
NG_023258.1:g.55577T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000703102.1:n.481T>A
ENST00000302326.5:c.3956T>A MANE Select ENSP00000304956.4:p.Leu1319Gln
ENST00000302326.4:c.3956T>A ENSP00000304956.4:p.Leu1319Gln
ENST00000424656.1:c.309T>A
ENST00000497225.1:n.312T>A
NM_002430.2:c.3956T>A NP_002421.3:p.Leu1319Gln
NM_002430.3:c.3956T>A MANE Select NP_002421.3:p.Leu1319Gln