Canonical Allele Identifier: CA2655934834
Gene: MN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750875A>G , CM000684.2:g.27750875A>G GRCh38
NC_000022.10:g.28146863A>G , CM000684.1:g.28146863A>G GRCh37
NC_000022.9:g.26476863A>G NCBI36
NG_023258.1:g.55624T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000703102.1:n.528T>C
ENST00000302326.5:c.*40T>C MANE Select ENSP00000304956.4:n.*40T>C
ENST00000302326.4:c.*40T>C ENSP00000304956.4:n.*40T>C
ENST00000424656.1:c.356T>C
ENST00000497225.1:n.359T>C
NM_002430.2:c.*40T>C NP_002421.3:n.*40T>C
NM_002430.3:c.*40T>C MANE Select NP_002421.3:n.*40T>C