Canonical Allele Identifier: CA2306872335
Gene: LMAN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.59359156C= , CM000680.2:g.59359156C= GRCh38
NC_000018.9:g.57026388C= , CM000680.1:g.57026388C= GRCh37
NC_000018.8:g.55177368C= NCBI36
NG_012097.1:g.5121G=

Transcript Alleles

HGVS Amino-acid change
ENST00000251047.6:c.89G= MANE Select ENSP00000251047.4:p.Gly30=
ENST00000251047.5:c.89G= ENSP00000251047.4:p.Gly30=
ENST00000587561.1:n.110G=
NM_005570.3:c.89G= NP_005561.1:p.Gly30=
NM_005570.4:c.89G= MANE Select NP_005561.1:p.Gly30=