Canonical Allele Identifier: CA402595791
Gene: LMAN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.57026397A>T (hg19) chr18:g.59359165A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.59359165A>T , CM000680.2:g.59359165A>T GRCh38
NC_000018.9:g.57026397A>T , CM000680.1:g.57026397A>T GRCh37
NC_000018.8:g.55177377A>T NCBI36
NG_012097.1:g.5112T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000251047.6:c.80T>A MANE Select ENSP00000251047.4:p.Phe27Tyr
ENST00000251047.5:c.80T>A ENSP00000251047.4:p.Phe27Tyr
ENST00000587561.1:n.101T>A
NM_005570.3:c.80T>A NP_005561.1:p.Phe27Tyr
NM_005570.4:c.80T>A MANE Select NP_005561.1:p.Phe27Tyr
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