Canonical Allele Identifier: CA2399817934
Gene: MN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750608T= , CM000684.2:g.27750608T= GRCh38
NC_000022.10:g.28146596T= , CM000684.1:g.28146596T= GRCh37
NC_000022.9:g.26476596T= NCBI36
NG_023258.1:g.55891A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000703102.1:n.795A=
ENST00000302326.5:c.*307A= MANE Select ENSP00000304956.4:n.*307A=
ENST00000302326.4:c.*307A= ENSP00000304956.4:n.*307A=
ENST00000424656.1:c.455+168A=
NM_002430.2:c.*307A= NP_002421.3:n.*307A=
NM_002430.3:c.*307A= MANE Select NP_002421.3:n.*307A=