Canonical Allele Identifier: CA2399818047
Gene: MN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750851_27750852delinsAG , CM000684.2:g.27750851_27750852delinsAG GRCh38
NC_000022.10:g.28146839_28146840delinsAG , CM000684.1:g.28146839_28146840delinsAG GRCh37
NC_000022.9:g.26476839_26476840delinsAG NCBI36
NG_023258.1:g.55647_55648delinsCT

Transcript Alleles

HGVS Amino-acid change
ENST00000703102.1:n.551_552delinsCT
ENST00000302326.5:c.*63_*64delinsCT MANE Select ENSP00000304956.4:n.*63_*64delinsCT
ENST00000302326.4:c.*63_*64delinsCT ENSP00000304956.4:n.*63_*64delinsCT
ENST00000424656.1:c.379_380delinsCT
ENST00000497225.1:n.382_383delinsCT
NM_002430.2:c.*63_*64delinsCT NP_002421.3:n.*63_*64delinsCT
NM_002430.3:c.*63_*64delinsCT MANE Select NP_002421.3:n.*63_*64delinsCT