Canonical Allele Identifier: CA2399818088
Gene: MN1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750900G= , CM000684.2:g.27750900G= GRCh38
NC_000022.10:g.28146888G= , CM000684.1:g.28146888G= GRCh37
NC_000022.9:g.26476888G= NCBI36
NG_023258.1:g.55599C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000703102.1:n.503C=
ENST00000302326.5:c.*15C= MANE Select ENSP00000304956.4:n.*15C=
ENST00000302326.4:c.*15C= ENSP00000304956.4:n.*15C=
ENST00000424656.1:c.331C=
ENST00000497225.1:n.334C=
NM_002430.2:c.*15C= NP_002421.3:n.*15C=
NM_002430.3:c.*15C= MANE Select NP_002421.3:n.*15C=
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