Canonical Allele Identifier: CA2306872338
Gene: LMAN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.59359161G= , CM000680.2:g.59359161G= GRCh38
NC_000018.9:g.57026393G= , CM000680.1:g.57026393G= GRCh37
NC_000018.8:g.55177373G= NCBI36
NG_012097.1:g.5116C=

Transcript Alleles

HGVS Amino-acid change
ENST00000251047.6:c.84C= MANE Select ENSP00000251047.4:p.Val28=
ENST00000251047.5:c.84C= ENSP00000251047.4:p.Val28=
ENST00000587561.1:n.105C=
NM_005570.3:c.84C= NP_005561.1:p.Val28=
NM_005570.4:c.84C= MANE Select NP_005561.1:p.Val28=