Canonical Allele Identifier: CA806484982

Gene: FABP6

Linked Data

• dbSNP Id: rs1202970439
• MyVariant Identifiers: chr5:g.159662768_159662770del (hg19) ; chr5:g.160235761_160235763del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.160235764_160235766del , CM000667.2:g.160235764_160235766del	GRCh38
NC_000005.9:g.159662771_159662773del , CM000667.1:g.159662771_159662773del	GRCh37
NC_000005.8:g.159595349_159595351del	NCBI36
NG_029500.1:g.53398_53400del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402432.4:c.333+855_333+857del MANE Select	ENSP00000385433.4:n.333+855_333+857del
ENST00000393980.8:c.480+855_480+857del	ENSP00000377549.4:n.480+855_480+857del
ENST00000402432.3:c.333+855_333+857del	ENSP00000385433.3:n.333+855_333+857del
ENST00000521362.1:n.329+855_329+857del
ENST00000523955.5:c.658+855_658+857del	ENSP00000428766.1:n.658+855_658+857del
NM_001040442.1:c.480+855_480+857del	NP_001035532.1:n.480+855_480+857del
NM_001130958.1:c.480+855_480+857del	NP_001124430.1:n.480+855_480+857del
NM_001445.2:c.333+855_333+857del	NP_001436.1:n.333+855_333+857del
XM_006714830.2:c.333+855_333+857del	XP_006714893.1:n.333+855_333+857del
XM_011534463.1:c.396+855_396+857del	XP_011532765.1:n.396+855_396+857del
NM_001130958.2:c.480+855_480+857del	NP_001124430.1:n.480+855_480+857del
NM_001445.3:c.333+855_333+857del MANE Select	NP_001436.1:n.333+855_333+857del