Canonical Allele Identifier: CA2655934813
Gene: MN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750845dup , CM000684.2:g.27750845dup GRCh38
NC_000022.10:g.28146833dup , CM000684.1:g.28146833dup GRCh37
NC_000022.9:g.26476833dup NCBI36
NG_023258.1:g.55655dup

Transcript Alleles

HGVS Amino-acid change
ENST00000703102.1:n.559dup
ENST00000302326.5:c.*71dup MANE Select ENSP00000304956.4:n.*71dup
ENST00000302326.4:c.*71dup ENSP00000304956.4:n.*71dup
ENST00000424656.1:c.387dup
ENST00000497225.1:n.390dup
NM_002430.2:c.*71dup NP_002421.3:n.*71dup
NM_002430.3:c.*71dup MANE Select NP_002421.3:n.*71dup