Canonical Allele Identifier: CA2474169132
Gene: FAAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46399224_46399225delinsGC , CM000663.2:g.46399224_46399225delinsGC GRCh38
NC_000001.10:g.46864896_46864897delinsGC , CM000663.1:g.46864896_46864897delinsGC GRCh37
NC_000001.9:g.46637483_46637484delinsGC NCBI36
NG_012195.1:g.9958_9959delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000243167.9:c.196-2867_196-2866delinsGC MANE Select ENSP00000243167.8:n.196-2867_196-2866delinsGC
ENST00000243167.8:c.196-2867_196-2866delinsGC ENSP00000243167.8:n.196-2867_196-2866delinsGC
ENST00000468718.5:n.216-2867_216-2866delinsGC
ENST00000493735.5:n.174-2867_174-2866delinsGC
NM_001441.2:c.196-2867_196-2866delinsGC NP_001432.2:n.196-2867_196-2866delinsGC
NM_001441.3:c.196-2867_196-2866delinsGC MANE Select NP_001432.2:n.196-2867_196-2866delinsGC