Canonical Allele Identifier: CA2655934749
Gene: MN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750794_27750796del , CM000684.2:g.27750794_27750796del GRCh38
NC_000022.10:g.28146782_28146784del , CM000684.1:g.28146782_28146784del GRCh37
NC_000022.9:g.26476782_26476784del NCBI36
NG_023258.1:g.55703_55705del

Transcript Alleles

HGVS Amino-acid Change
ENST00000703102.1:n.607_609del
ENST00000302326.5:c.*119_*121del MANE Select ENSP00000304956.4:n.*119_*121del
ENST00000302326.4:c.*119_*121del ENSP00000304956.4:n.*119_*121del
ENST00000424656.1:c.435_437del
ENST00000497225.1:n.438_440del
NM_002430.2:c.*119_*121del NP_002421.3:n.*119_*121del
NM_002430.3:c.*119_*121del MANE Select NP_002421.3:n.*119_*121del