Canonical Allele Identifier: CA2655934699
Gene: MN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750773_27750776del , CM000684.2:g.27750773_27750776del GRCh38
NC_000022.10:g.28146761_28146764del , CM000684.1:g.28146761_28146764del GRCh37
NC_000022.9:g.26476761_26476764del NCBI36
NG_023258.1:g.55726_55729del

Transcript Alleles

HGVS Amino-acid Change
ENST00000703102.1:n.630_633del
ENST00000302326.5:c.*142_*145del MANE Select ENSP00000304956.4:n.*142_*145del
ENST00000302326.4:c.*142_*145del ENSP00000304956.4:n.*142_*145del
ENST00000424656.1:c.455+3_455+6del
ENST00000497225.1:n.461_464del
NM_002430.2:c.*142_*145del NP_002421.3:n.*142_*145del
NM_002430.3:c.*142_*145del MANE Select NP_002421.3:n.*142_*145del