Canonical Allele Identifier: CA2399817887

Gene: MN1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.27750512_27750515delinsCTTA , CM000684.2:g.27750512_27750515delinsCTTA	GRCh38
NC_000022.10:g.28146500_28146503delinsCTTA , CM000684.1:g.28146500_28146503delinsCTTA	GRCh37
NC_000022.9:g.26476500_26476503delinsCTTA	NCBI36
NG_023258.1:g.55984_55987delinsTAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703102.1:n.888_891delinsTAAG
ENST00000302326.5:c.*400_*403delinsTAAG MANE Select	ENSP00000304956.4:n.*400_*403delinsTAAG
ENST00000302326.4:c.*400_*403delinsTAAG	ENSP00000304956.4:n.*400_*403delinsTAAG
ENST00000424656.1:c.455+261_455+264delinsTAAG
NM_002430.2:c.*400_*403delinsTAAG	NP_002421.3:n.*400_*403delinsTAAG
NM_002430.3:c.*400_*403delinsTAAG MANE Select	NP_002421.3:n.*400_*403delinsTAAG