Canonical Allele Identifier: CA2507479050
Gene: LMAN1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.59359257A>T , CM000680.2:g.59359257A>T GRCh38
NC_000018.9:g.57026489A>T , CM000680.1:g.57026489A>T GRCh37
NC_000018.8:g.55177469A>T NCBI36
NG_012097.1:g.5020T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000251047.6:c.-13T>A MANE Select ENSP00000251047.4:n.-13T>A
ENST00000251047.5:c.-13T>A ENSP00000251047.4:n.-13T>A
ENST00000587561.1:n.9T>A
NM_005570.3:c.-13T>A NP_005561.1:n.-13T>A
NM_005570.4:c.-13T>A MANE Select NP_005561.1:n.-13T>A
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