Canonical Allele Identifier: CA2399817964

Gene: MN1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.27750697_27750698delinsCT , CM000684.2:g.27750697_27750698delinsCT	GRCh38
NC_000022.10:g.28146685_28146686delinsCT , CM000684.1:g.28146685_28146686delinsCT	GRCh37
NC_000022.9:g.26476685_26476686delinsCT	NCBI36
NG_023258.1:g.55801_55802delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703102.1:n.705_706delinsAG
ENST00000302326.5:c.*217_*218delinsAG MANE Select	ENSP00000304956.4:n.*217_*218delinsAG
ENST00000302326.4:c.*217_*218delinsAG	ENSP00000304956.4:n.*217_*218delinsAG
ENST00000424656.1:c.455+78_455+79delinsAG
ENST00000497225.1:n.536_537delinsAG
NM_002430.2:c.*217_*218delinsAG	NP_002421.3:n.*217_*218delinsAG
NM_002430.3:c.*217_*218delinsAG MANE Select	NP_002421.3:n.*217_*218delinsAG