Canonical Allele Identifier: CA2399818040
Gene: MN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750836G= , CM000684.2:g.27750836G= GRCh38
NC_000022.10:g.28146824G= , CM000684.1:g.28146824G= GRCh37
NC_000022.9:g.26476824G= NCBI36
NG_023258.1:g.55663C=

Transcript Alleles

HGVS Amino-acid change
ENST00000703102.1:n.567C=
ENST00000302326.5:c.*79C= MANE Select ENSP00000304956.4:n.*79C=
ENST00000302326.4:c.*79C= ENSP00000304956.4:n.*79C=
ENST00000424656.1:c.395C=
ENST00000497225.1:n.398C=
NM_002430.2:c.*79C= NP_002421.3:n.*79C=
NM_002430.3:c.*79C= MANE Select NP_002421.3:n.*79C=