Canonical Allele Identifier: CA2655934739

Gene: MN1

Linked Data

• gnomAD v4: 22-27750785-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.27750785_27750786insG , CM000684.2:g.27750785_27750786insG	GRCh38
NC_000022.10:g.28146773_28146774insG , CM000684.1:g.28146773_28146774insG	GRCh37
NC_000022.9:g.26476773_26476774insG	NCBI36
NG_023258.1:g.55713_55714insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703102.1:n.617_618insC
ENST00000302326.5:c.*129_*130insC MANE Select	ENSP00000304956.4:n.*129_*130insC
ENST00000302326.4:c.*129_*130insC	ENSP00000304956.4:n.*129_*130insC
ENST00000424656.1:c.445_446insC
ENST00000497225.1:n.448_449insC
NM_002430.2:c.*129_*130insC	NP_002421.3:n.*129_*130insC
NM_002430.3:c.*129_*130insC MANE Select	NP_002421.3:n.*129_*130insC