Canonical Allele Identifier: CA2655934717

Gene: MN1

Linked Data

• gnomAD v4: 22-27750777-TAG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.27750781_27750782del , CM000684.2:g.27750781_27750782del	GRCh38
NC_000022.10:g.28146769_28146770del , CM000684.1:g.28146769_28146770del	GRCh37
NC_000022.9:g.26476769_26476770del	NCBI36
NG_023258.1:g.55720_55721del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703102.1:n.624_625del
ENST00000302326.5:c.*136_*137del MANE Select	ENSP00000304956.4:n.*136_*137del
ENST00000302326.4:c.*136_*137del	ENSP00000304956.4:n.*136_*137del
ENST00000424656.1:c.452_453del
ENST00000497225.1:n.455_456del
NM_002430.2:c.*136_*137del	NP_002421.3:n.*136_*137del
NM_002430.3:c.*136_*137del MANE Select	NP_002421.3:n.*136_*137del