Canonical Allele Identifier: CA2399818157
Gene: MN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27751061G= , CM000684.2:g.27751061G= GRCh38
NC_000022.10:g.28147049G= , CM000684.1:g.28147049G= GRCh37
NC_000022.9:g.26477049G= NCBI36
NG_023258.1:g.55438C=

Transcript Alleles

HGVS Amino-acid change
ENST00000703102.1:n.342C=
ENST00000302326.5:c.3817C= MANE Select ENSP00000304956.4:p.Gln1273=
ENST00000302326.4:c.3817C= ENSP00000304956.4:p.Gln1273=
ENST00000424656.1:c.170C=
ENST00000497225.1:n.173C=
NM_002430.2:c.3817C= NP_002421.3:p.Gln1273=
NM_002430.3:c.3817C= MANE Select NP_002421.3:p.Gln1273=