Canonical Allele Identifier: CA411032910
Gene: MN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750957G>T , CM000684.2:g.27750957G>T GRCh38
NC_000022.10:g.28146945G>T , CM000684.1:g.28146945G>T GRCh37
NC_000022.9:g.26476945G>T NCBI36
NG_023258.1:g.55542C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000703102.1:n.446C>A
ENST00000302326.5:c.3921C>A MANE Select ENSP00000304956.4:p.Asp1307Glu
ENST00000302326.4:c.3921C>A ENSP00000304956.4:p.Asp1307Glu
ENST00000424656.1:c.274C>A
ENST00000497225.1:n.277C>A
NM_002430.2:c.3921C>A NP_002421.3:p.Asp1307Glu
NM_002430.3:c.3921C>A MANE Select NP_002421.3:p.Asp1307Glu