Canonical Allele Identifier: CA920351000

Gene: MN1

Linked Data

• dbSNP Id: rs1568968720
• gnomAD v4: 22-27750578-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.27750584dup , CM000684.2:g.27750584dup	GRCh38
NC_000022.10:g.28146572dup , CM000684.1:g.28146572dup	GRCh37
NC_000022.9:g.26476572dup	NCBI36
NG_023258.1:g.55920dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703102.1:n.824dup
ENST00000302326.5:c.*336dup MANE Select	ENSP00000304956.4:n.*336dup
ENST00000302326.4:c.*336dup	ENSP00000304956.4:n.*336dup
ENST00000424656.1:c.455+197dup
NM_002430.2:c.*336dup	NP_002421.3:n.*336dup
NM_002430.3:c.*336dup MANE Select	NP_002421.3:n.*336dup