Canonical Allele Identifier: CA2655934722
Gene: MN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750779_27750781dup , CM000684.2:g.27750779_27750781dup GRCh38
NC_000022.10:g.28146767_28146769dup , CM000684.1:g.28146767_28146769dup GRCh37
NC_000022.9:g.26476767_26476769dup NCBI36
NG_023258.1:g.55718_55720dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000703102.1:n.622_624dup
ENST00000302326.5:c.*134_*136dup MANE Select ENSP00000304956.4:n.*134_*136dup
ENST00000302326.4:c.*134_*136dup ENSP00000304956.4:n.*134_*136dup
ENST00000424656.1:c.450_452dup
ENST00000497225.1:n.453_455dup
NM_002430.2:c.*134_*136dup NP_002421.3:n.*134_*136dup
NM_002430.3:c.*134_*136dup MANE Select NP_002421.3:n.*134_*136dup