Canonical Allele Identifier: CA2399818042
Gene: MN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750839G= , CM000684.2:g.27750839G= GRCh38
NC_000022.10:g.28146827G= , CM000684.1:g.28146827G= GRCh37
NC_000022.9:g.26476827G= NCBI36
NG_023258.1:g.55660C=

Transcript Alleles

HGVS Amino-acid change
ENST00000703102.1:n.564C=
ENST00000302326.5:c.*76C= MANE Select ENSP00000304956.4:n.*76C=
ENST00000302326.4:c.*76C= ENSP00000304956.4:n.*76C=
ENST00000424656.1:c.392C=
ENST00000497225.1:n.395C=
NM_002430.2:c.*76C= NP_002421.3:n.*76C=
NM_002430.3:c.*76C= MANE Select NP_002421.3:n.*76C=