Canonical Allele Identifier: CA2522784001
Gene: FAAH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46399226_46399227insTAAATAGGTGTTCTGTG , CM000663.2:g.46399226_46399227insTAAATAGGTGTTCTGTG GRCh38
NC_000001.10:g.46864898_46864899insTAAATAGGTGTTCTGTG , CM000663.1:g.46864898_46864899insTAAATAGGTGTTCTGTG GRCh37
NC_000001.9:g.46637485_46637486insTAAATAGGTGTTCTGTG NCBI36
NG_012195.1:g.9960_9961insTAAATAGGTGTTCTGTG

Transcript Alleles

HGVS Amino-acid change
ENST00000243167.9:c.196-2865_196-2864insTAAATAGGTGTTCTGTG MANE Select ENSP00000243167.8:n.196-2865_196-2864insTAAATAGGTGTTCTGTG
ENST00000243167.8:c.196-2865_196-2864insTAAATAGGTGTTCTGTG ENSP00000243167.8:n.196-2865_196-2864insTAAATAGGTGTTCTGTG
ENST00000468718.5:n.216-2865_216-2864insTAAATAGGTGTTCTGTG
ENST00000493735.5:n.174-2865_174-2864insTAAATAGGTGTTCTGTG
NM_001441.2:c.196-2865_196-2864insTAAATAGGTGTTCTGTG NP_001432.2:n.196-2865_196-2864insTAAATAGGTGTTCTGTG
NM_001441.3:c.196-2865_196-2864insTAAATAGGTGTTCTGTG MANE Select NP_001432.2:n.196-2865_196-2864insTAAATAGGTGTTCTGTG
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