Canonical Allele Identifier: CA1167798625

Gene: FAM151A ACOT11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.54609742_54609776delinsCAGCAAGGCCAGGGATGGCCGGAGGGCTGCGGGCT , CM000663.2:g.54609742_54609776delinsCAGCAAGGCCAGGGATGGCCGGAGGGCTGCGGGCT	GRCh38
NC_000001.10:g.55075415_55075449delinsCAGCAAGGCCAGGGATGGCCGGAGGGCTGCGGGCT , CM000663.1:g.55075415_55075449delinsCAGCAAGGCCAGGGATGGCCGGAGGGCTGCGGGCT	GRCh37
NC_000001.9:g.54848003_54848037delinsCAGCAAGGCCAGGGATGGCCGGAGGGCTGCGGGCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302250.7:c.1250_1284delinsAGCCCGCAGCCCTCCGGCCATCCCTGGCCTTGCTG (FAM151A) MANE Select	ENSP00000306888.2:p.Glu417=
ENST00000343744.7:c.*630_*664delinsCAGCAAGGCCAGGGATGGCCGGAGGGCTGCGGGCT (ACOT11) MANE Select	ENSP00000340260.2:n.*630_*664delinsCAGCAAGGCCAGGGATGGCCGGAGGG...
ENST00000302250.6:c.1250_1284delinsAGCCCGCAGCCCTCCGGCCATCCCTGGCCTTGCTG (FAM151A)	ENSP00000306888.2:p.Glu417=
ENST00000343744.6:c.*630_*664delinsCAGCAAGGCCAGGGATGGCCGGAGGGCTGCGGGCT (ACOT11)	ENSP00000340260.2:n.*630_*664delinsCAGCAAGGCCAGGGATGGCCGGAGGG...
ENST00000371304.2:c.918-229_918-195delinsAGCCCGCAGCCCTCCGGCCATCCCTGGCCTTGCTG (FAM151A)	ENSP00000360353.2:n.918-229_918-195delinsAGCCCGCAGCCCTCCGGCCA...
ENST00000371316.3:c.1629+1674_1629+1708delinsCAGCAAGGCCAGGGATGGCCGGAGGGCTGCGGGCT (ACOT11)	ENSP00000360366.3:n.1629+1674_1629+1708delinsCAGCAAGGCCAGGGAT...
ENST00000481208.5:n.2493_2527delinsCAGCAAGGCCAGGGATGGCCGGAGGGCTGCGGGCT (ACOT11)
NM_015547.3:c.1629+1674_1629+1708delinsCAGCAAGGCCAGGGATGGCCGGAGGGCTGCGGGCT (ACOT11)	NP_056362.1:n.1629+1674_1629+1708delinsCAGCAAGGCCAGGGATGGCCGG...
NM_147161.3:c.*630_*664delinsCAGCAAGGCCAGGGATGGCCGGAGGGCTGCGGGCT (ACOT11)	NP_671517.1:n.*630_*664delinsCAGCAAGGCCAGGGATGGCCGGAGGGCTGCGG...
NM_176782.2:c.1250_1284delinsAGCCCGCAGCCCTCCGGCCATCCCTGGCCTTGCTG (FAM151A)	NP_788954.2:p.Glu417=
XM_006710599.2:c.1172_1206delinsAGCCCGCAGCCCTCCGGCCATCCCTGGCCTTGCTG (FAM151A)	XP_006710662.1:p.Glu391=
XM_006710599.3:c.1172_1206delinsAGCCCGCAGCCCTCCGGCCATCCCTGGCCTTGCTG (FAM151A)	XP_006710662.1:p.Glu391=
NM_176782.3:c.1250_1284delinsAGCCCGCAGCCCTCCGGCCATCCCTGGCCTTGCTG (FAM151A) MANE Select	NP_788954.2:p.Glu417=
NM_015547.4:c.1629+1674_1629+1708delinsCAGCAAGGCCAGGGATGGCCGGAGGGCTGCGGGCT (ACOT11)	NP_056362.1:n.1629+1674_1629+1708delinsCAGCAAGGCCAGGGATGGCCGG...
NM_147161.4:c.*630_*664delinsCAGCAAGGCCAGGGATGGCCGGAGGGCTGCGGGCT (ACOT11) MANE Select	NP_671517.1:n.*630_*664delinsCAGCAAGGCCAGGGATGGCCGGAGGGCTGCGG...