Canonical Allele Identifier: CA2399818110
Gene: MN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750961G= , CM000684.2:g.27750961G= GRCh38
NC_000022.10:g.28146949G= , CM000684.1:g.28146949G= GRCh37
NC_000022.9:g.26476949G= NCBI36
NG_023258.1:g.55538C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000703102.1:n.442C=
ENST00000302326.5:c.3917C= MANE Select ENSP00000304956.4:p.Ser1306=
ENST00000302326.4:c.3917C= ENSP00000304956.4:p.Ser1306=
ENST00000424656.1:c.270C=
ENST00000497225.1:n.273C=
NM_002430.2:c.3917C= NP_002421.3:p.Ser1306=
NM_002430.3:c.3917C= MANE Select NP_002421.3:p.Ser1306=