Canonical Allele Identifier: CA2399817941
Gene: MN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750624G= , CM000684.2:g.27750624G= GRCh38
NC_000022.10:g.28146612G= , CM000684.1:g.28146612G= GRCh37
NC_000022.9:g.26476612G= NCBI36
NG_023258.1:g.55875C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000703102.1:n.779C=
ENST00000302326.5:c.*291C= MANE Select ENSP00000304956.4:n.*291C=
ENST00000302326.4:c.*291C= ENSP00000304956.4:n.*291C=
ENST00000424656.1:c.455+152C=
NM_002430.2:c.*291C= NP_002421.3:n.*291C=
NM_002430.3:c.*291C= MANE Select NP_002421.3:n.*291C=