Canonical Allele Identifier: CA2399818018

Gene: MN1

Linked Data

• dbSNP Id: rs1932756578

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.27750788_27750789insT , CM000684.2:g.27750788_27750789insT	GRCh38
NC_000022.10:g.28146776_28146777insT , CM000684.1:g.28146776_28146777insT	GRCh37
NC_000022.9:g.26476776_26476777insT	NCBI36
NG_023258.1:g.55710_55711insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703102.1:n.614_615insA
ENST00000302326.5:c.*126_*127insA MANE Select	ENSP00000304956.4:n.*126_*127insA
ENST00000302326.4:c.*126_*127insA	ENSP00000304956.4:n.*126_*127insA
ENST00000424656.1:c.442_443insA
ENST00000497225.1:n.445_446insA
NM_002430.2:c.*126_*127insA	NP_002421.3:n.*126_*127insA
NM_002430.3:c.*126_*127insA MANE Select	NP_002421.3:n.*126_*127insA