Canonical Allele Identifier: CA2717582111
Gene: FABP4 HGNC NCBI

Linked Data

dbSNP Id: rs2129790275

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.81478726del , CM000670.2:g.81478726del GRCh38
NC_000008.10:g.82390961del , CM000670.1:g.82390961del GRCh37
NC_000008.9:g.82553516del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256104.5:c.*140del MANE Select ENSP00000256104.4:n.*140del
ENST00000256104.4:c.*140del ENSP00000256104.4:n.*140del
ENST00000518669.5:n.474del
ENST00000521734.1:n.748del
ENST00000522659.1:c.*415del ENSP00000428385.1:n.*415del
NM_001442.2:c.*140del NP_001433.1:n.*140del
XR_001745980.1:n.514+16752del
NM_001442.3:c.*140del MANE Select NP_001433.1:n.*140del