Canonical Allele Identifier: CA1083564401

Gene: FABP6

Linked Data

• gnomAD v3: 5-160235681-GCCCT-G
• gnomAD v4: 5-160235681-GCCCT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.160235682_160235685del , CM000667.2:g.160235682_160235685del	GRCh38
NC_000005.9:g.159662689_159662692del , CM000667.1:g.159662689_159662692del	GRCh37
NC_000005.8:g.159595267_159595270del	NCBI36
NG_029500.1:g.53316_53319del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402432.4:c.333+773_333+776del MANE Select	ENSP00000385433.4:n.333+773_333+776del
ENST00000393980.8:c.480+773_480+776del	ENSP00000377549.4:n.480+773_480+776del
ENST00000402432.3:c.333+773_333+776del	ENSP00000385433.3:n.333+773_333+776del
ENST00000521362.1:n.329+773_329+776del
ENST00000523955.5:c.658+773_658+776del	ENSP00000428766.1:n.658+773_658+776del
NM_001040442.1:c.480+773_480+776del	NP_001035532.1:n.480+773_480+776del
NM_001130958.1:c.480+773_480+776del	NP_001124430.1:n.480+773_480+776del
NM_001445.2:c.333+773_333+776del	NP_001436.1:n.333+773_333+776del
XM_006714830.2:c.333+773_333+776del	XP_006714893.1:n.333+773_333+776del
XM_011534463.1:c.396+773_396+776del	XP_011532765.1:n.396+773_396+776del
NM_001130958.2:c.480+773_480+776del	NP_001124430.1:n.480+773_480+776del
NM_001445.3:c.333+773_333+776del MANE Select	NP_001436.1:n.333+773_333+776del