Canonical Allele Identifier: CA1797412182
Gene: FABP4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.81478707T= , CM000670.2:g.81478707T= GRCh38
NC_000008.10:g.82390942T= , CM000670.1:g.82390942T= GRCh37
NC_000008.9:g.82553497T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256104.5:c.*158A= MANE Select ENSP00000256104.4:n.*158A=
ENST00000256104.4:c.*158A= ENSP00000256104.4:n.*158A=
ENST00000518669.5:n.492A=
ENST00000522659.1:c.*433A= ENSP00000428385.1:n.*433A=
NM_001442.2:c.*158A= NP_001433.1:n.*158A=
XR_001745980.1:n.514+16733T=
NM_001442.3:c.*158A= MANE Select NP_001433.1:n.*158A=