Canonical Allele Identifier: CA2306872332
Gene: LMAN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.59359150C= , CM000680.2:g.59359150C= GRCh38
NC_000018.9:g.57026382C= , CM000680.1:g.57026382C= GRCh37
NC_000018.8:g.55177362C= NCBI36
NG_012097.1:g.5127G=

Transcript Alleles

HGVS Amino-acid change
ENST00000251047.6:c.95G= MANE Select ENSP00000251047.4:p.Gly32=
ENST00000251047.5:c.95G= ENSP00000251047.4:p.Gly32=
ENST00000587561.1:n.116G=
NM_005570.3:c.95G= NP_005561.1:p.Gly32=
NM_005570.4:c.95G= MANE Select NP_005561.1:p.Gly32=