Canonical Allele Identifier: CA2655934729

Gene: MN1

Linked Data

• gnomAD v4: 22-27750781-G-GGAAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.27750781_27750782insGAAAA , CM000684.2:g.27750781_27750782insGAAAA	GRCh38
NC_000022.10:g.28146769_28146770insGAAAA , CM000684.1:g.28146769_28146770insGAAAA	GRCh37
NC_000022.9:g.26476769_26476770insGAAAA	NCBI36
NG_023258.1:g.55717_55718insTTTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703102.1:n.621_622insTTTTC
ENST00000302326.5:c.*133_*134insTTTTC MANE Select	ENSP00000304956.4:n.*133_*134insTTTTC
ENST00000302326.4:c.*133_*134insTTTTC	ENSP00000304956.4:n.*133_*134insTTTTC
ENST00000424656.1:c.449_450insTTTTC
ENST00000497225.1:n.452_453insTTTTC
NM_002430.2:c.*133_*134insTTTTC	NP_002421.3:n.*133_*134insTTTTC
NM_002430.3:c.*133_*134insTTTTC MANE Select	NP_002421.3:n.*133_*134insTTTTC