Canonical Allele Identifier: CA1167798377

Gene: FAM151A ACOT11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.54609227_54609234delinsGCCTCCGC , CM000663.2:g.54609227_54609234delinsGCCTCCGC	GRCh38
NC_000001.10:g.55074900_55074907delinsGCCTCCGC , CM000663.1:g.55074900_55074907delinsGCCTCCGC	GRCh37
NC_000001.9:g.54847488_54847495delinsGCCTCCGC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302250.7:c.*34_*41delinsGCGGAGGC (FAM151A) MANE Select	ENSP00000306888.2:n.*34_*41delinsGCGGAGGC
ENST00000343744.7:c.*115_*122delinsGCCTCCGC (ACOT11) MANE Select	ENSP00000340260.2:n.*115_*122delinsGCCTCCGC
ENST00000302250.6:c.*34_*41delinsGCGGAGGC (FAM151A)	ENSP00000306888.2:n.*34_*41delinsGCGGAGGC
ENST00000343744.6:c.*115_*122delinsGCCTCCGC (ACOT11)	ENSP00000340260.2:n.*115_*122delinsGCCTCCGC
ENST00000371304.2:c.*34_*41delinsGCGGAGGC (FAM151A)	ENSP00000360353.2:n.*34_*41delinsGCGGAGGC
ENST00000371316.3:c.1629+1159_1629+1166delinsGCCTCCGC (ACOT11)	ENSP00000360366.3:n.1629+1159_1629+1166delinsGCCTCCGC
ENST00000481208.5:n.1978_1985delinsGCCTCCGC (ACOT11)
NM_015547.3:c.1629+1159_1629+1166delinsGCCTCCGC (ACOT11)	NP_056362.1:n.1629+1159_1629+1166delinsGCCTCCGC
NM_147161.3:c.*115_*122delinsGCCTCCGC (ACOT11)	NP_671517.1:n.*115_*122delinsGCCTCCGC
NM_176782.2:c.*34_*41delinsGCGGAGGC (FAM151A)	NP_788954.2:n.*34_*41delinsGCGGAGGC
XM_006710599.2:c.*34_*41delinsGCGGAGGC (FAM151A)	XP_006710662.1:n.*34_*41delinsGCGGAGGC
XM_006710599.3:c.*34_*41delinsGCGGAGGC (FAM151A)	XP_006710662.1:n.*34_*41delinsGCGGAGGC
NM_176782.3:c.*34_*41delinsGCGGAGGC (FAM151A) MANE Select	NP_788954.2:n.*34_*41delinsGCGGAGGC
NM_015547.4:c.1629+1159_1629+1166delinsGCCTCCGC (ACOT11)	NP_056362.1:n.1629+1159_1629+1166delinsGCCTCCGC
NM_147161.4:c.*115_*122delinsGCCTCCGC (ACOT11) MANE Select	NP_671517.1:n.*115_*122delinsGCCTCCGC