Canonical Allele Identifier: CA522177693

Gene: FABP3

Linked Data

• dbSNP Id: rs1197083571
• gnomAD v2: 1-31845774-C-CCGCGGCT
• gnomAD v4: 1-31372927-C-CCGCGGCT
• MyVariant Identifiers: chr1:g.31845774_31845775insCGCGGCT (hg19) ; chr1:g.31372927_31372928insCGCGGCT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.31372928_31372934dup , CM000663.2:g.31372928_31372934dup	GRCh38
NC_000001.10:g.31845775_31845781dup , CM000663.1:g.31845775_31845781dup	GRCh37
NC_000001.9:g.31618362_31618368dup	NCBI36
NG_047049.1:g.5350_5356dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373713.7:c.73+8_73+14dup MANE Select	ENSP00000362817.2:n.73+8_73+14dup
ENST00000373713.6:c.73+8_73+14dup	ENSP00000362817.2:n.73+8_73+14dup
ENST00000482018.1:c.73+8_73+14dup	ENSP00000473982.1:n.73+8_73+14dup
ENST00000498148.5:c.73+8_73+14dup	ENSP00000474078.1:n.73+8_73+14dup
NM_004102.3:c.73+8_73+14dup	NP_004093.1:n.73+8_73+14dup
XM_011541007.1:c.73+8_73+14dup	XP_011539309.1:n.73+8_73+14dup
NM_001320996.1:c.73+8_73+14dup	NP_001307925.1:n.73+8_73+14dup
NM_004102.4:c.73+8_73+14dup	NP_004093.1:n.73+8_73+14dup
XM_011541007.3:c.73+8_73+14dup	XP_011539309.1:n.73+8_73+14dup
NM_004102.5:c.73+8_73+14dup MANE Select	NP_004093.1:n.73+8_73+14dup
NM_001320996.2:c.73+8_73+14dup	NP_001307925.1:n.73+8_73+14dup