Canonical Allele Identifier: CA1001886363

Gene: FAM151A ACOT11

Linked Data

• dbSNP Id: rs1644078574
• gnomAD v3: 1-54609219-C-CCTGGCACAACTCTAGCATATCT
• gnomAD v4: 1-54609219-C-CCTGGCACAACTCTAGCATATCT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.54609219_54609220insCTGGCACAACTCTAGCATATCT , CM000663.2:g.54609219_54609220insCTGGCACAACTCTAGCATATCT	GRCh38
NC_000001.10:g.55074892_55074893insCTGGCACAACTCTAGCATATCT , CM000663.1:g.55074892_55074893insCTGGCACAACTCTAGCATATCT	GRCh37
NC_000001.9:g.54847480_54847481insCTGGCACAACTCTAGCATATCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302250.7:c.*48_*49insAGATATGCTAGAGTTGTGCCAG (FAM151A) MANE Select	ENSP00000306888.2:n.*48_*49insAGATATGCTAGAGTTGTGCCAG
ENST00000343744.7:c.*107_*108insCTGGCACAACTCTAGCATATCT (ACOT11) MANE Select	ENSP00000340260.2:n.*107_*108insCTGGCACAACTCTAGCATATCT
ENST00000302250.6:c.*48_*49insAGATATGCTAGAGTTGTGCCAG (FAM151A)	ENSP00000306888.2:n.*48_*49insAGATATGCTAGAGTTGTGCCAG
ENST00000343744.6:c.*107_*108insCTGGCACAACTCTAGCATATCT (ACOT11)	ENSP00000340260.2:n.*107_*108insCTGGCACAACTCTAGCATATCT
ENST00000371304.2:c.*48_*49insAGATATGCTAGAGTTGTGCCAG (FAM151A)	ENSP00000360353.2:n.*48_*49insAGATATGCTAGAGTTGTGCCAG
ENST00000371316.3:c.1629+1151_1629+1152insCTGGCACAACTCTAGCATATCT (ACOT11)	ENSP00000360366.3:n.1629+1151_1629+1152insCTGGCACAACTCTAGCATA...
ENST00000481208.5:n.1970_1971insCTGGCACAACTCTAGCATATCT (ACOT11)
NM_015547.3:c.1629+1151_1629+1152insCTGGCACAACTCTAGCATATCT (ACOT11)	NP_056362.1:n.1629+1151_1629+1152insCTGGCACAACTCTAGCATATCT
NM_147161.3:c.*107_*108insCTGGCACAACTCTAGCATATCT (ACOT11)	NP_671517.1:n.*107_*108insCTGGCACAACTCTAGCATATCT
NM_176782.2:c.*48_*49insAGATATGCTAGAGTTGTGCCAG (FAM151A)	NP_788954.2:n.*48_*49insAGATATGCTAGAGTTGTGCCAG
XM_006710599.2:c.*48_*49insAGATATGCTAGAGTTGTGCCAG (FAM151A)	XP_006710662.1:n.*48_*49insAGATATGCTAGAGTTGTGCCAG
XM_006710599.3:c.*48_*49insAGATATGCTAGAGTTGTGCCAG (FAM151A)	XP_006710662.1:n.*48_*49insAGATATGCTAGAGTTGTGCCAG
NM_176782.3:c.*48_*49insAGATATGCTAGAGTTGTGCCAG (FAM151A) MANE Select	NP_788954.2:n.*48_*49insAGATATGCTAGAGTTGTGCCAG
NM_015547.4:c.1629+1151_1629+1152insCTGGCACAACTCTAGCATATCT (ACOT11)	NP_056362.1:n.1629+1151_1629+1152insCTGGCACAACTCTAGCATATCT
NM_147161.4:c.*107_*108insCTGGCACAACTCTAGCATATCT (ACOT11) MANE Select	NP_671517.1:n.*107_*108insCTGGCACAACTCTAGCATATCT