Canonical Allele Identifier: CA2306872392
Gene: LMAN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.59359243A= , CM000680.2:g.59359243A= GRCh38
NC_000018.9:g.57026475A= , CM000680.1:g.57026475A= GRCh37
NC_000018.8:g.55177455A= NCBI36
NG_012097.1:g.5034T=

Transcript Alleles

HGVS Amino-acid change
ENST00000251047.6:c.2T= MANE Select ENSP00000251047.4:p.Met1=
ENST00000251047.5:c.2T= ENSP00000251047.4:p.Met1=
ENST00000587561.1:n.23T=
NM_005570.3:c.2T= NP_005561.1:p.Met1=
NM_005570.4:c.2T= MANE Select NP_005561.1:p.Met1=