Canonical Allele Identifier: CA2818640084
Gene: MN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750860_27750866del , CM000684.2:g.27750860_27750866del GRCh38
NC_000022.10:g.28146848_28146854del , CM000684.1:g.28146848_28146854del GRCh37
NC_000022.9:g.26476848_26476854del NCBI36
NG_023258.1:g.55635_55641del

Transcript Alleles

HGVS Amino-acid Change
ENST00000703102.1:n.539_545del
ENST00000302326.5:c.*51_*57del MANE Select ENSP00000304956.4:n.*51_*57del
ENST00000302326.4:c.*51_*57del ENSP00000304956.4:n.*51_*57del
ENST00000424656.1:c.367_373del
ENST00000497225.1:n.370_376del
NM_002430.2:c.*51_*57del NP_002421.3:n.*51_*57del
NM_002430.3:c.*51_*57del MANE Select NP_002421.3:n.*51_*57del