Canonical Allele Identifier: CA411033550
Gene: MN1 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000703102.1:n.361A>C
ENST00000302326.5:c.3836A>C MANE Select ENSP00000304956.4:p.Gln1279Pro
ENST00000302326.4:c.3836A>C ENSP00000304956.4:p.Gln1279Pro
ENST00000424656.1:c.189A>C
ENST00000497225.1:n.192A>C
NM_002430.2:c.3836A>C NP_002421.3:p.Gln1279Pro
NM_002430.3:c.3836A>C MANE Select NP_002421.3:p.Gln1279Pro