Canonical Allele Identifier: CA2399818050
Gene: MN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750853G= , CM000684.2:g.27750853G= GRCh38
NC_000022.10:g.28146841G= , CM000684.1:g.28146841G= GRCh37
NC_000022.9:g.26476841G= NCBI36
NG_023258.1:g.55646C=

Transcript Alleles

HGVS Amino-acid change
ENST00000703102.1:n.550C=
ENST00000302326.5:c.*62C= MANE Select ENSP00000304956.4:n.*62C=
ENST00000302326.4:c.*62C= ENSP00000304956.4:n.*62C=
ENST00000424656.1:c.378C=
ENST00000497225.1:n.381C=
NM_002430.2:c.*62C= NP_002421.3:n.*62C=
NM_002430.3:c.*62C= MANE Select NP_002421.3:n.*62C=