Canonical Allele Identifier: CA2399818051
Gene: MN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750856G= , CM000684.2:g.27750856G= GRCh38
NC_000022.10:g.28146844G= , CM000684.1:g.28146844G= GRCh37
NC_000022.9:g.26476844G= NCBI36
NG_023258.1:g.55643C=

Transcript Alleles

HGVS Amino-acid change
ENST00000703102.1:n.547C=
ENST00000302326.5:c.*59C= MANE Select ENSP00000304956.4:n.*59C=
ENST00000302326.4:c.*59C= ENSP00000304956.4:n.*59C=
ENST00000424656.1:c.375C=
ENST00000497225.1:n.378C=
NM_002430.2:c.*59C= NP_002421.3:n.*59C=
NM_002430.3:c.*59C= MANE Select NP_002421.3:n.*59C=