Canonical Allele Identifier: CA2306872401
Gene: LMAN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.59359254T= , CM000680.2:g.59359254T= GRCh38
NC_000018.9:g.57026486T= , CM000680.1:g.57026486T= GRCh37
NC_000018.8:g.55177466T= NCBI36
NG_012097.1:g.5023A=

Transcript Alleles

HGVS Amino-acid change
ENST00000251047.6:c.-10A= MANE Select ENSP00000251047.4:n.-10A=
ENST00000251047.5:c.-10A= ENSP00000251047.4:n.-10A=
ENST00000587561.1:n.12A=
NM_005570.3:c.-10A= NP_005561.1:n.-10A=
NM_005570.4:c.-10A= MANE Select NP_005561.1:n.-10A=