Canonical Allele Identifier: CA2399817923
Gene: MN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750589T= , CM000684.2:g.27750589T= GRCh38
NC_000022.10:g.28146577T= , CM000684.1:g.28146577T= GRCh37
NC_000022.9:g.26476577T= NCBI36
NG_023258.1:g.55910A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000703102.1:n.814A=
ENST00000302326.5:c.*326A= MANE Select ENSP00000304956.4:n.*326A=
ENST00000302326.4:c.*326A= ENSP00000304956.4:n.*326A=
ENST00000424656.1:c.455+187A=
NM_002430.2:c.*326A= NP_002421.3:n.*326A=
NM_002430.3:c.*326A= MANE Select NP_002421.3:n.*326A=