Canonical Allele Identifier: CA1167798568

Gene: FAM151A ACOT11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.54609611_54609638delinsGGGAAGACCTCAGCCACAGCTGTAAGCA , CM000663.2:g.54609611_54609638delinsGGGAAGACCTCAGCCACAGCTGTAAGCA	GRCh38
NC_000001.10:g.55075284_55075311delinsGGGAAGACCTCAGCCACAGCTGTAAGCA , CM000663.1:g.55075284_55075311delinsGGGAAGACCTCAGCCACAGCTGTAAGCA	GRCh37
NC_000001.9:g.54847872_54847899delinsGGGAAGACCTCAGCCACAGCTGTAAGCA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302250.7:c.1388_1415delinsTGCTTACAGCTGTGGCTGAGGTCTTCCC (FAM151A) MANE Select	ENSP00000306888.2:p.Leu463=
ENST00000343744.7:c.*499_*526delinsGGGAAGACCTCAGCCACAGCTGTAAGCA (ACOT11) MANE Select	ENSP00000340260.2:n.*499_*526delinsGGGAAGACCTCAGCCACAGCTGTAAG...
ENST00000302250.6:c.1388_1415delinsTGCTTACAGCTGTGGCTGAGGTCTTCCC (FAM151A)	ENSP00000306888.2:p.Leu463=
ENST00000343744.6:c.*499_*526delinsGGGAAGACCTCAGCCACAGCTGTAAGCA (ACOT11)	ENSP00000340260.2:n.*499_*526delinsGGGAAGACCTCAGCCACAGCTGTAAG...
ENST00000371304.2:c.918-91_918-64delinsTGCTTACAGCTGTGGCTGAGGTCTTCCC (FAM151A)	ENSP00000360353.2:n.918-91_918-64delinsTGCTTACAGCTGTGGCTGAGGT...
ENST00000371316.3:c.1629+1543_1629+1570delinsGGGAAGACCTCAGCCACAGCTGTAAGCA (ACOT11)	ENSP00000360366.3:n.1629+1543_1629+1570delinsGGGAAGACCTCAGCCA...
ENST00000481208.5:n.2362_2389delinsGGGAAGACCTCAGCCACAGCTGTAAGCA (ACOT11)
NM_015547.3:c.1629+1543_1629+1570delinsGGGAAGACCTCAGCCACAGCTGTAAGCA (ACOT11)	NP_056362.1:n.1629+1543_1629+1570delinsGGGAAGACCTCAGCCACAGCTG...
NM_147161.3:c.*499_*526delinsGGGAAGACCTCAGCCACAGCTGTAAGCA (ACOT11)	NP_671517.1:n.*499_*526delinsGGGAAGACCTCAGCCACAGCTGTAAGCA
NM_176782.2:c.1388_1415delinsTGCTTACAGCTGTGGCTGAGGTCTTCCC (FAM151A)	NP_788954.2:p.Leu463=
XM_006710599.2:c.1310_1337delinsTGCTTACAGCTGTGGCTGAGGTCTTCCC (FAM151A)	XP_006710662.1:p.Leu437=
XM_006710599.3:c.1310_1337delinsTGCTTACAGCTGTGGCTGAGGTCTTCCC (FAM151A)	XP_006710662.1:p.Leu437=
NM_176782.3:c.1388_1415delinsTGCTTACAGCTGTGGCTGAGGTCTTCCC (FAM151A) MANE Select	NP_788954.2:p.Leu463=
NM_015547.4:c.1629+1543_1629+1570delinsGGGAAGACCTCAGCCACAGCTGTAAGCA (ACOT11)	NP_056362.1:n.1629+1543_1629+1570delinsGGGAAGACCTCAGCCACAGCTG...
NM_147161.4:c.*499_*526delinsGGGAAGACCTCAGCCACAGCTGTAAGCA (ACOT11) MANE Select	NP_671517.1:n.*499_*526delinsGGGAAGACCTCAGCCACAGCTGTAAGCA