Canonical Allele Identifier: CA920350995

Gene: MN1

Linked Data

• dbSNP Id: rs1568968670

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.27750451del , CM000684.2:g.27750451del	GRCh38
NC_000022.10:g.28146439del , CM000684.1:g.28146439del	GRCh37
NC_000022.9:g.26476439del	NCBI36
NG_023258.1:g.56052del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703102.1:n.956del
ENST00000302326.5:c.*468del MANE Select	ENSP00000304956.4:n.*468del
ENST00000302326.4:c.*468del	ENSP00000304956.4:n.*468del
ENST00000424656.1:c.456-219del
NM_002430.2:c.*468del	NP_002421.3:n.*468del
NM_002430.3:c.*468del MANE Select	NP_002421.3:n.*468del