Canonical Allele Identifier: CA2399818095
Gene: MN1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750912C= , CM000684.2:g.27750912C= GRCh38
NC_000022.10:g.28146900C= , CM000684.1:g.28146900C= GRCh37
NC_000022.9:g.26476900C= NCBI36
NG_023258.1:g.55587G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000703102.1:n.491G=
ENST00000302326.5:c.*3G= MANE Select ENSP00000304956.4:n.*3G=
ENST00000302326.4:c.*3G= ENSP00000304956.4:n.*3G=
ENST00000424656.1:c.319G=
ENST00000497225.1:n.322G=
NM_002430.2:c.*3G= NP_002421.3:n.*3G=
NM_002430.3:c.*3G= MANE Select NP_002421.3:n.*3G=
Search 100 bp 5'
Search 100 bp 3'