Canonical Allele Identifier: CA1797412238
Gene: FABP4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.81478760T= , CM000670.2:g.81478760T= GRCh38
NC_000008.10:g.82390995T= , CM000670.1:g.82390995T= GRCh37
NC_000008.9:g.82553550T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256104.5:c.*105A= MANE Select ENSP00000256104.4:n.*105A=
ENST00000256104.4:c.*105A= ENSP00000256104.4:n.*105A=
ENST00000518669.5:n.439A=
ENST00000521734.1:n.713A=
ENST00000522659.1:c.*380A= ENSP00000428385.1:n.*380A=
NM_001442.2:c.*105A= NP_001433.1:n.*105A=
XR_001745980.1:n.514+16786T=
NM_001442.3:c.*105A= MANE Select NP_001433.1:n.*105A=
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