Canonical Allele Identifier: CA2399818149
Gene: MN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27751039C= , CM000684.2:g.27751039C= GRCh38
NC_000022.10:g.28147027C= , CM000684.1:g.28147027C= GRCh37
NC_000022.9:g.26477027C= NCBI36
NG_023258.1:g.55460G=

Transcript Alleles

HGVS Amino-acid change
ENST00000703102.1:n.364G=
ENST00000302326.5:c.3839G= MANE Select ENSP00000304956.4:p.Cys1280=
ENST00000302326.4:c.3839G= ENSP00000304956.4:p.Cys1280=
ENST00000424656.1:c.192G=
ENST00000497225.1:n.195G=
NM_002430.2:c.3839G= NP_002421.3:p.Cys1280=
NM_002430.3:c.3839G= MANE Select NP_002421.3:p.Cys1280=