Canonical Allele Identifier: CA130830369

Gene: FABP6

Linked Data

• dbSNP Id: rs141776542
• gnomAD v2: 5-159662780-TTCTC-T
• gnomAD v3: 5-160235773-TTCTC-T
• gnomAD v4: 5-160235773-TTCTC-T
• MyVariant Identifiers: chr5:g.159662787_159662790del (hg19) ; chr5:g.159662781_159662784del (hg19) ; chr5:g.160235780_160235783del (hg38) ; chr5:g.160235774_160235777del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.160235788_160235791del , CM000667.2:g.160235788_160235791del	GRCh38
NC_000005.9:g.159662795_159662798del , CM000667.1:g.159662795_159662798del	GRCh37
NC_000005.8:g.159595373_159595376del	NCBI36
NG_029500.1:g.53422_53425del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402432.4:c.333+879_333+882del MANE Select	ENSP00000385433.4:n.333+879_333+882del
ENST00000393980.8:c.480+879_480+882del	ENSP00000377549.4:n.480+879_480+882del
ENST00000402432.3:c.333+879_333+882del	ENSP00000385433.3:n.333+879_333+882del
ENST00000521362.1:n.329+879_329+882del
ENST00000523955.5:c.658+879_658+882del	ENSP00000428766.1:n.658+879_658+882del
NM_001040442.1:c.480+879_480+882del	NP_001035532.1:n.480+879_480+882del
NM_001130958.1:c.480+879_480+882del	NP_001124430.1:n.480+879_480+882del
NM_001445.2:c.333+879_333+882del	NP_001436.1:n.333+879_333+882del
XM_006714830.2:c.333+879_333+882del	XP_006714893.1:n.333+879_333+882del
XM_011534463.1:c.396+879_396+882del	XP_011532765.1:n.396+879_396+882del
NM_001130958.2:c.480+879_480+882del	NP_001124430.1:n.480+879_480+882del
NM_001445.3:c.333+879_333+882del MANE Select	NP_001436.1:n.333+879_333+882del