Canonical Allele Identifier: CA2841376795

Gene: FAM151A ACOT11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.54609360_54609362del , CM000663.2:g.54609360_54609362del	GRCh38
NC_000001.10:g.55075033_55075035del , CM000663.1:g.55075033_55075035del	GRCh37
NC_000001.9:g.54847621_54847623del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302250.7:c.1666_1668del (FAM151A) MANE Select	ENSP00000306888.2:p.Leu556del
ENST00000343744.7:c.*248_*250del (ACOT11) MANE Select	ENSP00000340260.2:n.*248_*250del
ENST00000302250.6:c.1666_1668del (FAM151A)	ENSP00000306888.2:p.Leu556del
ENST00000343744.6:c.*248_*250del (ACOT11)	ENSP00000340260.2:n.*248_*250del
ENST00000371304.2:c.1105_1107del (FAM151A)	ENSP00000360353.2:p.Leu369del
ENST00000371316.3:c.1629+1292_1629+1294del (ACOT11)	ENSP00000360366.3:n.1629+1292_1629+1294del
ENST00000481208.5:n.2111_2113del (ACOT11)
NM_015547.3:c.1629+1292_1629+1294del (ACOT11)	NP_056362.1:n.1629+1292_1629+1294del
NM_147161.3:c.*248_*250del (ACOT11)	NP_671517.1:n.*248_*250del
NM_176782.2:c.1666_1668del (FAM151A)	NP_788954.2:p.Leu556del
XM_006710599.2:c.1588_1590del (FAM151A)	XP_006710662.1:p.Leu530del
XM_006710599.3:c.1588_1590del (FAM151A)	XP_006710662.1:p.Leu530del
NM_176782.3:c.1666_1668del (FAM151A) MANE Select	NP_788954.2:p.Leu556del
NM_015547.4:c.1629+1292_1629+1294del (ACOT11)	NP_056362.1:n.1629+1292_1629+1294del
NM_147161.4:c.*248_*250del (ACOT11) MANE Select	NP_671517.1:n.*248_*250del