Canonical Allele Identifier: CA2399817939
Gene: MN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750621G= , CM000684.2:g.27750621G= GRCh38
NC_000022.10:g.28146609G= , CM000684.1:g.28146609G= GRCh37
NC_000022.9:g.26476609G= NCBI36
NG_023258.1:g.55878C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000703102.1:n.782C=
ENST00000302326.5:c.*294C= MANE Select ENSP00000304956.4:n.*294C=
ENST00000302326.4:c.*294C= ENSP00000304956.4:n.*294C=
ENST00000424656.1:c.455+155C=
NM_002430.2:c.*294C= NP_002421.3:n.*294C=
NM_002430.3:c.*294C= MANE Select NP_002421.3:n.*294C=