Canonical Allele Identifier: CA564031618

Gene: FABP6

Linked Data

• dbSNP Id: rs1162406041
• gnomAD v2: 5-159662792-CT-C
• gnomAD v3: 5-160235785-CT-C
• gnomAD v4: 5-160235785-CT-C
• MyVariant Identifiers: chr5:g.159662793del (hg19) ; chr5:g.160235786del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.160235786del , CM000667.2:g.160235786del	GRCh38
NC_000005.9:g.159662793del , CM000667.1:g.159662793del	GRCh37
NC_000005.8:g.159595371del	NCBI36
NG_029500.1:g.53420del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402432.4:c.333+877del MANE Select	ENSP00000385433.4:n.333+877del
ENST00000393980.8:c.480+877del	ENSP00000377549.4:n.480+877del
ENST00000402432.3:c.333+877del	ENSP00000385433.3:n.333+877del
ENST00000521362.1:n.329+877del
ENST00000523955.5:c.658+877del	ENSP00000428766.1:n.658+877del
NM_001040442.1:c.480+877del	NP_001035532.1:n.480+877del
NM_001130958.1:c.480+877del	NP_001124430.1:n.480+877del
NM_001445.2:c.333+877del	NP_001436.1:n.333+877del
XM_006714830.2:c.333+877del	XP_006714893.1:n.333+877del
XM_011534463.1:c.396+877del	XP_011532765.1:n.396+877del
NM_001130958.2:c.480+877del	NP_001124430.1:n.480+877del
NM_001445.3:c.333+877del MANE Select	NP_001436.1:n.333+877del