Canonical Allele Identifier: CA2818640083
Gene: MN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750854G>T , CM000684.2:g.27750854G>T GRCh38
NC_000022.10:g.28146842G>T , CM000684.1:g.28146842G>T GRCh37
NC_000022.9:g.26476842G>T NCBI36
NG_023258.1:g.55645C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000703102.1:n.549C>A
ENST00000302326.5:c.*61C>A MANE Select ENSP00000304956.4:n.*61C>A
ENST00000302326.4:c.*61C>A ENSP00000304956.4:n.*61C>A
ENST00000424656.1:c.377C>A
ENST00000497225.1:n.380C>A
NM_002430.2:c.*61C>A NP_002421.3:n.*61C>A
NM_002430.3:c.*61C>A MANE Select NP_002421.3:n.*61C>A