Canonical Allele Identifier: CA411033521
Gene: MN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27751037G>T , CM000684.2:g.27751037G>T GRCh38
NC_000022.10:g.28147025G>T , CM000684.1:g.28147025G>T GRCh37
NC_000022.9:g.26477025G>T NCBI36
NG_023258.1:g.55462C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000703102.1:n.366C>A
ENST00000302326.5:c.3841C>A MANE Select ENSP00000304956.4:p.Leu1281Met
ENST00000302326.4:c.3841C>A ENSP00000304956.4:p.Leu1281Met
ENST00000424656.1:c.194C>A
ENST00000497225.1:n.197C>A
NM_002430.2:c.3841C>A NP_002421.3:p.Leu1281Met
NM_002430.3:c.3841C>A MANE Select NP_002421.3:p.Leu1281Met