Canonical Allele Identifier: CA2399817876
Gene: MN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750502C= , CM000684.2:g.27750502C= GRCh38
NC_000022.10:g.28146490C= , CM000684.1:g.28146490C= GRCh37
NC_000022.9:g.26476490C= NCBI36
NG_023258.1:g.55997G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000703102.1:n.901G=
ENST00000302326.5:c.*413G= MANE Select ENSP00000304956.4:n.*413G=
ENST00000302326.4:c.*413G= ENSP00000304956.4:n.*413G=
ENST00000424656.1:c.456-274G=
NM_002430.2:c.*413G= NP_002421.3:n.*413G=
NM_002430.3:c.*413G= MANE Select NP_002421.3:n.*413G=