Canonical Allele Identifier: CA1797412166
Gene: FABP4 HGNC NCBI

Linked Data

dbSNP Id: rs1808008964

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.81478705del , CM000670.2:g.81478705del GRCh38
NC_000008.10:g.82390940del , CM000670.1:g.82390940del GRCh37
NC_000008.9:g.82553495del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256104.5:c.*166del MANE Select ENSP00000256104.4:n.*166del
ENST00000256104.4:c.*166del ENSP00000256104.4:n.*166del
ENST00000518669.5:n.500del
ENST00000522659.1:c.*441del ENSP00000428385.1:n.*441del
NM_001442.2:c.*166del NP_001433.1:n.*166del
XR_001745980.1:n.514+16731del
NM_001442.3:c.*166del MANE Select NP_001433.1:n.*166del