Canonical Allele Identifier: CA2399818061

Gene: MN1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.27750869_27750870delinsAG , CM000684.2:g.27750869_27750870delinsAG	GRCh38
NC_000022.10:g.28146857_28146858delinsAG , CM000684.1:g.28146857_28146858delinsAG	GRCh37
NC_000022.9:g.26476857_26476858delinsAG	NCBI36
NG_023258.1:g.55629_55630delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000703102.1:n.533_534delinsCT
ENST00000302326.5:c.*45_*46delinsCT MANE Select	ENSP00000304956.4:n.*45_*46delinsCT
ENST00000302326.4:c.*45_*46delinsCT	ENSP00000304956.4:n.*45_*46delinsCT
ENST00000424656.1:c.361_362delinsCT
ENST00000497225.1:n.364_365delinsCT
NM_002430.2:c.*45_*46delinsCT	NP_002421.3:n.*45_*46delinsCT
NM_002430.3:c.*45_*46delinsCT MANE Select	NP_002421.3:n.*45_*46delinsCT