Canonical Allele Identifier: CA1167798551

Gene: FAM151A ACOT11

Linked Data

• dbSNP Id: rs1644086902

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.54609580_54609582del , CM000663.2:g.54609580_54609582del	GRCh38
NC_000001.10:g.55075253_55075255del , CM000663.1:g.55075253_55075255del	GRCh37
NC_000001.9:g.54847841_54847843del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302250.7:c.1448_1450del (FAM151A) MANE Select	ENSP00000306888.2:p.Glu483del
ENST00000343744.7:c.*468_*470del (ACOT11) MANE Select	ENSP00000340260.2:n.*468_*470del
ENST00000302250.6:c.1448_1450del (FAM151A)	ENSP00000306888.2:p.Glu483del
ENST00000343744.6:c.*468_*470del (ACOT11)	ENSP00000340260.2:n.*468_*470del
ENST00000371304.2:c.918-31_918-29del (FAM151A)	ENSP00000360353.2:n.918-31_918-29del
ENST00000371316.3:c.1629+1512_1629+1514del (ACOT11)	ENSP00000360366.3:n.1629+1512_1629+1514del
ENST00000481208.5:n.2331_2333del (ACOT11)
NM_015547.3:c.1629+1512_1629+1514del (ACOT11)	NP_056362.1:n.1629+1512_1629+1514del
NM_147161.3:c.*468_*470del (ACOT11)	NP_671517.1:n.*468_*470del
NM_176782.2:c.1448_1450del (FAM151A)	NP_788954.2:p.Glu483del
XM_006710599.2:c.1370_1372del (FAM151A)	XP_006710662.1:p.Glu457del
XM_006710599.3:c.1370_1372del (FAM151A)	XP_006710662.1:p.Glu457del
NM_176782.3:c.1448_1450del (FAM151A) MANE Select	NP_788954.2:p.Glu483del
NM_015547.4:c.1629+1512_1629+1514del (ACOT11)	NP_056362.1:n.1629+1512_1629+1514del
NM_147161.4:c.*468_*470del (ACOT11) MANE Select	NP_671517.1:n.*468_*470del