Canonical Allele Identifier: CA2399817847

Gene: MN1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.27750440_27750441delinsAC , CM000684.2:g.27750440_27750441delinsAC	GRCh38
NC_000022.10:g.28146428_28146429delinsAC , CM000684.1:g.28146428_28146429delinsAC	GRCh37
NC_000022.9:g.26476428_26476429delinsAC	NCBI36
NG_023258.1:g.56058_56059delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703102.1:n.962_963delinsGT
ENST00000302326.5:c.*474_*475delinsGT MANE Select	ENSP00000304956.4:n.*474_*475delinsGT
ENST00000302326.4:c.*474_*475delinsGT	ENSP00000304956.4:n.*474_*475delinsGT
ENST00000424656.1:c.456-213_456-212delinsGT
NM_002430.2:c.*474_*475delinsGT	NP_002421.3:n.*474_*475delinsGT
NM_002430.3:c.*474_*475delinsGT MANE Select	NP_002421.3:n.*474_*475delinsGT