Canonical Allele Identifier: CA411032799
Gene: MN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750943A>T , CM000684.2:g.27750943A>T GRCh38
NC_000022.10:g.28146931A>T , CM000684.1:g.28146931A>T GRCh37
NC_000022.9:g.26476931A>T NCBI36
NG_023258.1:g.55556T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000703102.1:n.460T>A
ENST00000302326.5:c.3935T>A MANE Select ENSP00000304956.4:p.Phe1312Tyr
ENST00000302326.4:c.3935T>A ENSP00000304956.4:p.Phe1312Tyr
ENST00000424656.1:c.288T>A
ENST00000497225.1:n.291T>A
NM_002430.2:c.3935T>A NP_002421.3:p.Phe1312Tyr
NM_002430.3:c.3935T>A MANE Select NP_002421.3:p.Phe1312Tyr