Canonical Allele Identifier: CA402595792
Gene: LMAN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.57026398A>T (hg19) chr18:g.59359166A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.59359166A>T , CM000680.2:g.59359166A>T GRCh38
NC_000018.9:g.57026398A>T , CM000680.1:g.57026398A>T GRCh37
NC_000018.8:g.55177378A>T NCBI36
NG_012097.1:g.5111T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000251047.6:c.79T>A MANE Select ENSP00000251047.4:p.Phe27Ile
ENST00000251047.5:c.79T>A ENSP00000251047.4:p.Phe27Ile
ENST00000587561.1:n.100T>A
NM_005570.3:c.79T>A NP_005561.1:p.Phe27Ile
NM_005570.4:c.79T>A MANE Select NP_005561.1:p.Phe27Ile
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