Canonical Allele Identifier: CA2399817996

Gene: MN1

Linked Data

• dbSNP Id: rs1932756242

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.27750754_27750757dup , CM000684.2:g.27750754_27750757dup	GRCh38
NC_000022.10:g.28146742_28146745dup , CM000684.1:g.28146742_28146745dup	GRCh37
NC_000022.9:g.26476742_26476745dup	NCBI36
NG_023258.1:g.55742_55745dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703102.1:n.646_649dup
ENST00000302326.5:c.*158_*161dup MANE Select	ENSP00000304956.4:n.*158_*161dup
ENST00000302326.4:c.*158_*161dup	ENSP00000304956.4:n.*158_*161dup
ENST00000424656.1:c.455+19_455+22dup
ENST00000497225.1:n.477_480dup
NM_002430.2:c.*158_*161dup	NP_002421.3:n.*158_*161dup
NM_002430.3:c.*158_*161dup MANE Select	NP_002421.3:n.*158_*161dup