Canonical Allele Identifier: CA2399817918
Gene: MN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750582A= , CM000684.2:g.27750582A= GRCh38
NC_000022.10:g.28146570A= , CM000684.1:g.28146570A= GRCh37
NC_000022.9:g.26476570A= NCBI36
NG_023258.1:g.55917T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000703102.1:n.821T=
ENST00000302326.5:c.*333T= MANE Select ENSP00000304956.4:n.*333T=
ENST00000302326.4:c.*333T= ENSP00000304956.4:n.*333T=
ENST00000424656.1:c.455+194T=
NM_002430.2:c.*333T= NP_002421.3:n.*333T=
NM_002430.3:c.*333T= MANE Select NP_002421.3:n.*333T=