Canonical Allele Identifier: CA1067271730
Gene: FABP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320694_119320695insAAAAATTCTTACCCTGAGTTCAGTTCCGTCTGCTAGG , CM000666.2:g.119320694_119320695insAAAAATTCTTACCCTGAGTTCAGTTCCGTCTGCTAGG GRCh38
NC_000004.11:g.120241849_120241850insAAAAATTCTTACCCTGAGTTCAGTTCCGTCTGCTAGG , CM000666.1:g.120241849_120241850insAAAAATTCTTACCCTGAGTTCAGTTCCGTCTGCTAGG GRCh37
NC_000004.10:g.120461297_120461298insAAAAATTCTTACCCTGAGTTCAGTTCCGTCTGCTAGG NCBI36
NG_011444.1:g.6467_6468insCCTAGCAGACGGAACTGAACTCAGGGTAAGAATTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000274024.4:c.215_216insCCTAGCAGACGGAACTGAACTCAGGGTAAGAATTTTT MANE Select ENSP00000274024.3:p.Gly81ValfsTer10
ENST00000274024.3:c.215_216insCCTAGCAGACGGAACTGAACTCAGGGTAAGAATTTTT ENSP00000274024.3:p.Gly81ValfsTer10
NM_000134.3:c.215_216insCCTAGCAGACGGAACTGAACTCAGGGTAAGAATTTTT NP_000125.2:p.Gly81ValfsTer10
NM_000134.4:c.215_216insCCTAGCAGACGGAACTGAACTCAGGGTAAGAATTTTT MANE Select NP_000125.2:p.Gly81ValfsTer10