Canonical Allele Identifier: CA1797412177
Gene: FABP4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.81478704A= , CM000670.2:g.81478704A= GRCh38
NC_000008.10:g.82390939A= , CM000670.1:g.82390939A= GRCh37
NC_000008.9:g.82553494A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256104.5:c.*161T= MANE Select ENSP00000256104.4:n.*161T=
ENST00000256104.4:c.*161T= ENSP00000256104.4:n.*161T=
ENST00000518669.5:n.495T=
ENST00000522659.1:c.*436T= ENSP00000428385.1:n.*436T=
NM_001442.2:c.*161T= NP_001433.1:n.*161T=
XR_001745980.1:n.514+16730A=
NM_001442.3:c.*161T= MANE Select NP_001433.1:n.*161T=