Canonical Allele Identifier: CA2645794465

Gene: FAM151A ACOT11

Linked Data

• gnomAD v4: 1-54609667-CGAAA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.54609668_54609671del , CM000663.2:g.54609668_54609671del	GRCh38
NC_000001.10:g.55075341_55075344del , CM000663.1:g.55075341_55075344del	GRCh37
NC_000001.9:g.54847929_54847932del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302250.7:c.1355_1358del (FAM151A) MANE Select	ENSP00000306888.2:p.Phe452TrpfsTer22
ENST00000343744.7:c.*556_*559del (ACOT11) MANE Select	ENSP00000340260.2:n.*556_*559del
ENST00000302250.6:c.1355_1358del (FAM151A)	ENSP00000306888.2:p.Phe452TrpfsTer22
ENST00000343744.6:c.*556_*559del (ACOT11)	ENSP00000340260.2:n.*556_*559del
ENST00000371304.2:c.918-124_918-121del (FAM151A)	ENSP00000360353.2:n.918-124_918-121del
ENST00000371316.3:c.1629+1600_1629+1603del (ACOT11)	ENSP00000360366.3:n.1629+1600_1629+1603del
ENST00000481208.5:n.2419_2422del (ACOT11)
NM_015547.3:c.1629+1600_1629+1603del (ACOT11)	NP_056362.1:n.1629+1600_1629+1603del
NM_147161.3:c.*556_*559del (ACOT11)	NP_671517.1:n.*556_*559del
NM_176782.2:c.1355_1358del (FAM151A)	NP_788954.2:p.Phe452TrpfsTer22
XM_006710599.2:c.1277_1280del (FAM151A)	XP_006710662.1:p.Phe426TrpfsTer22
XM_006710599.3:c.1277_1280del (FAM151A)	XP_006710662.1:p.Phe426TrpfsTer22
NM_176782.3:c.1355_1358del (FAM151A) MANE Select	NP_788954.2:p.Phe452TrpfsTer22
NM_015547.4:c.1629+1600_1629+1603del (ACOT11)	NP_056362.1:n.1629+1600_1629+1603del
NM_147161.4:c.*556_*559del (ACOT11) MANE Select	NP_671517.1:n.*556_*559del