Canonical Allele Identifier: CA2399817943
Gene: MN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750629A= , CM000684.2:g.27750629A= GRCh38
NC_000022.10:g.28146617A= , CM000684.1:g.28146617A= GRCh37
NC_000022.9:g.26476617A= NCBI36
NG_023258.1:g.55870T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000703102.1:n.774T=
ENST00000302326.5:c.*286T= MANE Select ENSP00000304956.4:n.*286T=
ENST00000302326.4:c.*286T= ENSP00000304956.4:n.*286T=
ENST00000424656.1:c.455+147T=
NM_002430.2:c.*286T= NP_002421.3:n.*286T=
NM_002430.3:c.*286T= MANE Select NP_002421.3:n.*286T=