Canonical Allele Identifier: CA1595452607

Gene: FABP6

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.160235655_160235656delinsTG , CM000667.2:g.160235655_160235656delinsTG	GRCh38
NC_000005.9:g.159662662_159662663delinsTG , CM000667.1:g.159662662_159662663delinsTG	GRCh37
NC_000005.8:g.159595240_159595241delinsTG	NCBI36
NG_029500.1:g.53289_53290delinsTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000402432.4:c.333+746_333+747delinsTG MANE Select	ENSP00000385433.4:n.333+746_333+747delinsTG
ENST00000393980.8:c.480+746_480+747delinsTG	ENSP00000377549.4:n.480+746_480+747delinsTG
ENST00000402432.3:c.333+746_333+747delinsTG	ENSP00000385433.3:n.333+746_333+747delinsTG
ENST00000521362.1:n.329+746_329+747delinsTG
ENST00000523955.5:c.658+746_658+747delinsTG	ENSP00000428766.1:n.658+746_658+747delinsTG
NM_001040442.1:c.480+746_480+747delinsTG	NP_001035532.1:n.480+746_480+747delinsTG
NM_001130958.1:c.480+746_480+747delinsTG	NP_001124430.1:n.480+746_480+747delinsTG
NM_001445.2:c.333+746_333+747delinsTG	NP_001436.1:n.333+746_333+747delinsTG
XM_006714830.2:c.333+746_333+747delinsTG	XP_006714893.1:n.333+746_333+747delinsTG
XM_011534463.1:c.396+746_396+747delinsTG	XP_011532765.1:n.396+746_396+747delinsTG
NM_001130958.2:c.480+746_480+747delinsTG	NP_001124430.1:n.480+746_480+747delinsTG
NM_001445.3:c.333+746_333+747delinsTG MANE Select	NP_001436.1:n.333+746_333+747delinsTG