Canonical Allele Identifier: CA1167798459

Gene: FAM151A ACOT11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.54609388_54609389delinsGC , CM000663.2:g.54609388_54609389delinsGC	GRCh38
NC_000001.10:g.55075061_55075062delinsGC , CM000663.1:g.55075061_55075062delinsGC	GRCh37
NC_000001.9:g.54847649_54847650delinsGC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302250.7:c.1637_1638delinsGC (FAM151A) MANE Select	ENSP00000306888.2:p.Gly546=
ENST00000343744.7:c.*276_*277delinsGC (ACOT11) MANE Select	ENSP00000340260.2:n.*276_*277delinsGC
ENST00000302250.6:c.1637_1638delinsGC (FAM151A)	ENSP00000306888.2:p.Gly546=
ENST00000343744.6:c.*276_*277delinsGC (ACOT11)	ENSP00000340260.2:n.*276_*277delinsGC
ENST00000371304.2:c.1076_1077delinsGC (FAM151A)	ENSP00000360353.2:p.Gly359=
ENST00000371316.3:c.1629+1320_1629+1321delinsGC (ACOT11)	ENSP00000360366.3:n.1629+1320_1629+1321delinsGC
ENST00000481208.5:n.2139_2140delinsGC (ACOT11)
NM_015547.3:c.1629+1320_1629+1321delinsGC (ACOT11)	NP_056362.1:n.1629+1320_1629+1321delinsGC
NM_147161.3:c.*276_*277delinsGC (ACOT11)	NP_671517.1:n.*276_*277delinsGC
NM_176782.2:c.1637_1638delinsGC (FAM151A)	NP_788954.2:p.Gly546=
XM_006710599.2:c.1559_1560delinsGC (FAM151A)	XP_006710662.1:p.Gly520=
XM_006710599.3:c.1559_1560delinsGC (FAM151A)	XP_006710662.1:p.Gly520=
NM_176782.3:c.1637_1638delinsGC (FAM151A) MANE Select	NP_788954.2:p.Gly546=
NM_015547.4:c.1629+1320_1629+1321delinsGC (ACOT11)	NP_056362.1:n.1629+1320_1629+1321delinsGC
NM_147161.4:c.*276_*277delinsGC (ACOT11) MANE Select	NP_671517.1:n.*276_*277delinsGC