Canonical Allele Identifier: CA411033547
Gene: MN1 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000703102.1:n.361A>T
ENST00000302326.5:c.3836A>T MANE Select ENSP00000304956.4:p.Gln1279Leu
ENST00000302326.4:c.3836A>T ENSP00000304956.4:p.Gln1279Leu
ENST00000424656.1:c.189A>T
ENST00000497225.1:n.192A>T
NM_002430.2:c.3836A>T NP_002421.3:p.Gln1279Leu
NM_002430.3:c.3836A>T MANE Select NP_002421.3:p.Gln1279Leu