Canonical Allele Identifier: CA1595452613

Gene: FABP6

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.160235665_160235666delinsTG , CM000667.2:g.160235665_160235666delinsTG	GRCh38
NC_000005.9:g.159662672_159662673delinsTG , CM000667.1:g.159662672_159662673delinsTG	GRCh37
NC_000005.8:g.159595250_159595251delinsTG	NCBI36
NG_029500.1:g.53299_53300delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402432.4:c.333+756_333+757delinsTG MANE Select	ENSP00000385433.4:n.333+756_333+757delinsTG
ENST00000393980.8:c.480+756_480+757delinsTG	ENSP00000377549.4:n.480+756_480+757delinsTG
ENST00000402432.3:c.333+756_333+757delinsTG	ENSP00000385433.3:n.333+756_333+757delinsTG
ENST00000521362.1:n.329+756_329+757delinsTG
ENST00000523955.5:c.658+756_658+757delinsTG	ENSP00000428766.1:n.658+756_658+757delinsTG
NM_001040442.1:c.480+756_480+757delinsTG	NP_001035532.1:n.480+756_480+757delinsTG
NM_001130958.1:c.480+756_480+757delinsTG	NP_001124430.1:n.480+756_480+757delinsTG
NM_001445.2:c.333+756_333+757delinsTG	NP_001436.1:n.333+756_333+757delinsTG
XM_006714830.2:c.333+756_333+757delinsTG	XP_006714893.1:n.333+756_333+757delinsTG
XM_011534463.1:c.396+756_396+757delinsTG	XP_011532765.1:n.396+756_396+757delinsTG
NM_001130958.2:c.480+756_480+757delinsTG	NP_001124430.1:n.480+756_480+757delinsTG
NM_001445.3:c.333+756_333+757delinsTG MANE Select	NP_001436.1:n.333+756_333+757delinsTG