Canonical Allele Identifier: CA2399818108
Gene: MN1 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000703102.1:n.446C=
ENST00000302326.5:c.3921C= MANE Select ENSP00000304956.4:p.Asp1307=
ENST00000302326.4:c.3921C= ENSP00000304956.4:p.Asp1307=
ENST00000424656.1:c.274C=
ENST00000497225.1:n.277C=
NM_002430.2:c.3921C= NP_002421.3:p.Asp1307=
NM_002430.3:c.3921C= MANE Select NP_002421.3:p.Asp1307=