Canonical Allele Identifier: CA1083564419

Gene: FABP6

Linked Data

• gnomAD v3: 5-160235687-C-CG
• gnomAD v4: 5-160235687-C-CG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.160235687_160235688insG , CM000667.2:g.160235687_160235688insG	GRCh38
NC_000005.9:g.159662694_159662695insG , CM000667.1:g.159662694_159662695insG	GRCh37
NC_000005.8:g.159595272_159595273insG	NCBI36
NG_029500.1:g.53321_53322insG

Transcript Alleles

HGVS	Amino-acid change
ENST00000402432.4:c.333+778_333+779insG MANE Select	ENSP00000385433.4:n.333+778_333+779insG
ENST00000393980.8:c.480+778_480+779insG	ENSP00000377549.4:n.480+778_480+779insG
ENST00000402432.3:c.333+778_333+779insG	ENSP00000385433.3:n.333+778_333+779insG
ENST00000521362.1:n.329+778_329+779insG
ENST00000523955.5:c.658+778_658+779insG	ENSP00000428766.1:n.658+778_658+779insG
NM_001040442.1:c.480+778_480+779insG	NP_001035532.1:n.480+778_480+779insG
NM_001130958.1:c.480+778_480+779insG	NP_001124430.1:n.480+778_480+779insG
NM_001445.2:c.333+778_333+779insG	NP_001436.1:n.333+778_333+779insG
XM_006714830.2:c.333+778_333+779insG	XP_006714893.1:n.333+778_333+779insG
XM_011534463.1:c.396+778_396+779insG	XP_011532765.1:n.396+778_396+779insG
NM_001130958.2:c.480+778_480+779insG	NP_001124430.1:n.480+778_480+779insG
NM_001445.3:c.333+778_333+779insG MANE Select	NP_001436.1:n.333+778_333+779insG