Canonical Allele Identifier: CA2597249488
Gene: FAAH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46399238_46399246dup , CM000663.2:g.46399238_46399246dup GRCh38
NC_000001.10:g.46864910_46864918dup , CM000663.1:g.46864910_46864918dup GRCh37
NC_000001.9:g.46637497_46637505dup NCBI36
NG_012195.1:g.9972_9980dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000243167.9:c.196-2853_196-2845dup MANE Select ENSP00000243167.8:n.196-2853_196-2845dup
ENST00000243167.8:c.196-2853_196-2845dup ENSP00000243167.8:n.196-2853_196-2845dup
ENST00000468718.5:n.216-2853_216-2845dup
ENST00000493735.5:n.174-2853_174-2845dup
NM_001441.2:c.196-2853_196-2845dup NP_001432.2:n.196-2853_196-2845dup
NM_001441.3:c.196-2853_196-2845dup MANE Select NP_001432.2:n.196-2853_196-2845dup