Canonical Allele Identifier: CA1024815636
Gene: MN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750843T>A , CM000684.2:g.27750843T>A GRCh38
NC_000022.10:g.28146831T>A , CM000684.1:g.28146831T>A GRCh37
NC_000022.9:g.26476831T>A NCBI36
NG_023258.1:g.55656A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000703102.1:n.560A>T
ENST00000302326.5:c.*72A>T MANE Select ENSP00000304956.4:n.*72A>T
ENST00000302326.4:c.*72A>T ENSP00000304956.4:n.*72A>T
ENST00000424656.1:c.388A>T
ENST00000497225.1:n.391A>T
NM_002430.2:c.*72A>T NP_002421.3:n.*72A>T
NM_002430.3:c.*72A>T MANE Select NP_002421.3:n.*72A>T