Canonical Allele Identifier: CA2399818068
Gene: MN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750878G= , CM000684.2:g.27750878G= GRCh38
NC_000022.10:g.28146866G= , CM000684.1:g.28146866G= GRCh37
NC_000022.9:g.26476866G= NCBI36
NG_023258.1:g.55621C=

Transcript Alleles

HGVS Amino-acid change
ENST00000703102.1:n.525C=
ENST00000302326.5:c.*37C= MANE Select ENSP00000304956.4:n.*37C=
ENST00000302326.4:c.*37C= ENSP00000304956.4:n.*37C=
ENST00000424656.1:c.353C=
ENST00000497225.1:n.356C=
NM_002430.2:c.*37C= NP_002421.3:n.*37C=
NM_002430.3:c.*37C= MANE Select NP_002421.3:n.*37C=