Canonical Allele Identifier: CA2399818054
Gene: MN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750859G= , CM000684.2:g.27750859G= GRCh38
NC_000022.10:g.28146847G= , CM000684.1:g.28146847G= GRCh37
NC_000022.9:g.26476847G= NCBI36
NG_023258.1:g.55640C=

Transcript Alleles

HGVS Amino-acid change
ENST00000703102.1:n.544C=
ENST00000302326.5:c.*56C= MANE Select ENSP00000304956.4:n.*56C=
ENST00000302326.4:c.*56C= ENSP00000304956.4:n.*56C=
ENST00000424656.1:c.372C=
ENST00000497225.1:n.375C=
NM_002430.2:c.*56C= NP_002421.3:n.*56C=
NM_002430.3:c.*56C= MANE Select NP_002421.3:n.*56C=