Canonical Allele Identifier: CA2399817889

Gene: MN1

Linked Data

• dbSNP Id: rs1932754301

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.27750517_27750519del , CM000684.2:g.27750517_27750519del	GRCh38
NC_000022.10:g.28146505_28146507del , CM000684.1:g.28146505_28146507del	GRCh37
NC_000022.9:g.26476505_26476507del	NCBI36
NG_023258.1:g.55984_55986del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703102.1:n.888_890del
ENST00000302326.5:c.*400_*402del MANE Select	ENSP00000304956.4:n.*400_*402del
ENST00000302326.4:c.*400_*402del	ENSP00000304956.4:n.*400_*402del
ENST00000424656.1:c.455+261_455+263del
NM_002430.2:c.*400_*402del	NP_002421.3:n.*400_*402del
NM_002430.3:c.*400_*402del MANE Select	NP_002421.3:n.*400_*402del