Canonical Allele Identifier: CA2306872403
Gene: LMAN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.59359259C= , CM000680.2:g.59359259C= GRCh38
NC_000018.9:g.57026491C= , CM000680.1:g.57026491C= GRCh37
NC_000018.8:g.55177471C= NCBI36
NG_012097.1:g.5018G=

Transcript Alleles

HGVS Amino-acid change
ENST00000251047.6:c.-15G= MANE Select ENSP00000251047.4:n.-15G=
ENST00000251047.5:c.-15G= ENSP00000251047.4:n.-15G=
ENST00000587561.1:n.7G=
NM_005570.3:c.-15G= NP_005561.1:n.-15G=
NM_005570.4:c.-15G= MANE Select NP_005561.1:n.-15G=