Canonical Allele Identifier: CA2655934758
Gene: MN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750798T>G , CM000684.2:g.27750798T>G GRCh38
NC_000022.10:g.28146786T>G , CM000684.1:g.28146786T>G GRCh37
NC_000022.9:g.26476786T>G NCBI36
NG_023258.1:g.55701A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000703102.1:n.605A>C
ENST00000302326.5:c.*117A>C MANE Select ENSP00000304956.4:n.*117A>C
ENST00000302326.4:c.*117A>C ENSP00000304956.4:n.*117A>C
ENST00000424656.1:c.433A>C
ENST00000497225.1:n.436A>C
NM_002430.2:c.*117A>C NP_002421.3:n.*117A>C
NM_002430.3:c.*117A>C MANE Select NP_002421.3:n.*117A>C