Canonical Allele Identifier: CA2655934313

Gene: MN1

Linked Data

• gnomAD v4: 22-27750470-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.27750470G>A , CM000684.2:g.27750470G>A	GRCh38
NC_000022.10:g.28146458G>A , CM000684.1:g.28146458G>A	GRCh37
NC_000022.9:g.26476458G>A	NCBI36
NG_023258.1:g.56029C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703102.1:n.933C>T
ENST00000302326.5:c.*445C>T MANE Select	ENSP00000304956.4:n.*445C>T
ENST00000302326.4:c.*445C>T	ENSP00000304956.4:n.*445C>T
ENST00000424656.1:c.456-242C>T
NM_002430.2:c.*445C>T	NP_002421.3:n.*445C>T
NM_002430.3:c.*445C>T MANE Select	NP_002421.3:n.*445C>T