Canonical Allele Identifier: CA2362973014
Gene: LBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.38363210_38363212delinsCAT , CM000682.2:g.38363210_38363212delinsCAT GRCh38
NC_000020.10:g.36991864_36991866delinsCAT , CM000682.1:g.36991864_36991866delinsCAT GRCh37
NC_000020.9:g.36425278_36425280delinsCAT NCBI36
NG_034239.1:g.21800_21802delinsCAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000217407.3:c.653-765_653-763delinsCAT MANE Select ENSP00000217407.2:n.653-765_653-763delinsCAT
ENST00000217407.2:c.653-765_653-763delinsCAT ENSP00000217407.2:n.653-765_653-763delinsCAT
NM_004139.4:c.653-765_653-763delinsCAT NP_004130.2:n.653-765_653-763delinsCAT
NM_004139.5:c.653-765_653-763delinsCAT MANE Select NP_004130.2:n.653-765_653-763delinsCAT