Canonical Allele Identifier: CA2362973120
Gene: LBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.38363455_38363456delinsAG , CM000682.2:g.38363455_38363456delinsAG GRCh38
NC_000020.10:g.36992109_36992110delinsAG , CM000682.1:g.36992109_36992110delinsAG GRCh37
NC_000020.9:g.36425523_36425524delinsAG NCBI36
NG_034239.1:g.22045_22046delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000217407.3:c.653-520_653-519delinsAG MANE Select ENSP00000217407.2:n.653-520_653-519delinsAG
ENST00000217407.2:c.653-520_653-519delinsAG ENSP00000217407.2:n.653-520_653-519delinsAG
NM_004139.4:c.653-520_653-519delinsAG NP_004130.2:n.653-520_653-519delinsAG
NM_004139.5:c.653-520_653-519delinsAG MANE Select NP_004130.2:n.653-520_653-519delinsAG