Canonical Allele Identifier: CA411033510
Gene: MN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27751034A>T , CM000684.2:g.27751034A>T GRCh38
NC_000022.10:g.28147022A>T , CM000684.1:g.28147022A>T GRCh37
NC_000022.9:g.26477022A>T NCBI36
NG_023258.1:g.55465T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000703102.1:n.369T>A
ENST00000302326.5:c.3844T>A MANE Select ENSP00000304956.4:p.Ser1282Thr
ENST00000302326.4:c.3844T>A ENSP00000304956.4:p.Ser1282Thr
ENST00000424656.1:c.197T>A
ENST00000497225.1:n.200T>A
NM_002430.2:c.3844T>A NP_002421.3:p.Ser1282Thr
NM_002430.3:c.3844T>A MANE Select NP_002421.3:p.Ser1282Thr