Canonical Allele Identifier: CA1167798358

Gene: FAM151A ACOT11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.54609202_54609206delinsATTTC , CM000663.2:g.54609202_54609206delinsATTTC	GRCh38
NC_000001.10:g.55074875_55074879delinsATTTC , CM000663.1:g.55074875_55074879delinsATTTC	GRCh37
NC_000001.9:g.54847463_54847467delinsATTTC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302250.7:c.*62_*66delinsGAAAT (FAM151A) MANE Select	ENSP00000306888.2:n.*62_*66delinsGAAAT
ENST00000343744.7:c.*90_*94delinsATTTC (ACOT11) MANE Select	ENSP00000340260.2:n.*90_*94delinsATTTC
ENST00000302250.6:c.*62_*66delinsGAAAT (FAM151A)	ENSP00000306888.2:n.*62_*66delinsGAAAT
ENST00000343744.6:c.*90_*94delinsATTTC (ACOT11)	ENSP00000340260.2:n.*90_*94delinsATTTC
ENST00000371304.2:c.*62_*66delinsGAAAT (FAM151A)	ENSP00000360353.2:n.*62_*66delinsGAAAT
ENST00000371316.3:c.1629+1134_1629+1138delinsATTTC (ACOT11)	ENSP00000360366.3:n.1629+1134_1629+1138delinsATTTC
ENST00000481208.5:n.1953_1957delinsATTTC (ACOT11)
NM_015547.3:c.1629+1134_1629+1138delinsATTTC (ACOT11)	NP_056362.1:n.1629+1134_1629+1138delinsATTTC
NM_147161.3:c.*90_*94delinsATTTC (ACOT11)	NP_671517.1:n.*90_*94delinsATTTC
NM_176782.2:c.*62_*66delinsGAAAT (FAM151A)	NP_788954.2:n.*62_*66delinsGAAAT
XM_006710599.2:c.*62_*66delinsGAAAT (FAM151A)	XP_006710662.1:n.*62_*66delinsGAAAT
XM_006710599.3:c.*62_*66delinsGAAAT (FAM151A)	XP_006710662.1:n.*62_*66delinsGAAAT
NM_176782.3:c.*62_*66delinsGAAAT (FAM151A) MANE Select	NP_788954.2:n.*62_*66delinsGAAAT
NM_015547.4:c.1629+1134_1629+1138delinsATTTC (ACOT11)	NP_056362.1:n.1629+1134_1629+1138delinsATTTC
NM_147161.4:c.*90_*94delinsATTTC (ACOT11) MANE Select	NP_671517.1:n.*90_*94delinsATTTC