Canonical Allele Identifier: CA2306872399
Gene: LMAN1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.59359251T= , CM000680.2:g.59359251T= GRCh38
NC_000018.9:g.57026483T= , CM000680.1:g.57026483T= GRCh37
NC_000018.8:g.55177463T= NCBI36
NG_012097.1:g.5026A=

Transcript Alleles

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