Canonical Allele Identifier: CA411033552
Gene: MN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27751042T>C , CM000684.2:g.27751042T>C GRCh38
NC_000022.10:g.28147030T>C , CM000684.1:g.28147030T>C GRCh37
NC_000022.9:g.26477030T>C NCBI36
NG_023258.1:g.55457A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000703102.1:n.361A>G
ENST00000302326.5:c.3836A>G MANE Select ENSP00000304956.4:p.Gln1279Arg
ENST00000302326.4:c.3836A>G ENSP00000304956.4:p.Gln1279Arg
ENST00000424656.1:c.189A>G
ENST00000497225.1:n.192A>G
NM_002430.2:c.3836A>G NP_002421.3:p.Gln1279Arg
NM_002430.3:c.3836A>G MANE Select NP_002421.3:p.Gln1279Arg