Canonical Allele Identifier: CA2306872337
Gene: LMAN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.59359160G= , CM000680.2:g.59359160G= GRCh38
NC_000018.9:g.57026392G= , CM000680.1:g.57026392G= GRCh37
NC_000018.8:g.55177372G= NCBI36
NG_012097.1:g.5117C=

Transcript Alleles

HGVS Amino-acid change
ENST00000251047.6:c.85C= MANE Select ENSP00000251047.4:p.Arg29=
ENST00000251047.5:c.85C= ENSP00000251047.4:p.Arg29=
ENST00000587561.1:n.106C=
NM_005570.3:c.85C= NP_005561.1:p.Arg29=
NM_005570.4:c.85C= MANE Select NP_005561.1:p.Arg29=