Canonical Allele Identifier: CA1167798417

Gene: FAM151A ACOT11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.54609296_54609297delinsTC , CM000663.2:g.54609296_54609297delinsTC	GRCh38
NC_000001.10:g.55074969_55074970delinsTC , CM000663.1:g.55074969_55074970delinsTC	GRCh37
NC_000001.9:g.54847557_54847558delinsTC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302250.7:c.1729_1730delinsGA (FAM151A) MANE Select	ENSP00000306888.2:p.Asp577=
ENST00000343744.7:c.*184_*185delinsTC (ACOT11) MANE Select	ENSP00000340260.2:n.*184_*185delinsTC
ENST00000302250.6:c.1729_1730delinsGA (FAM151A)	ENSP00000306888.2:p.Asp577=
ENST00000343744.6:c.*184_*185delinsTC (ACOT11)	ENSP00000340260.2:n.*184_*185delinsTC
ENST00000371304.2:c.1168_1169delinsGA (FAM151A)	ENSP00000360353.2:p.Asp390=
ENST00000371316.3:c.1629+1228_1629+1229delinsTC (ACOT11)	ENSP00000360366.3:n.1629+1228_1629+1229delinsTC
ENST00000481208.5:n.2047_2048delinsTC (ACOT11)
NM_015547.3:c.1629+1228_1629+1229delinsTC (ACOT11)	NP_056362.1:n.1629+1228_1629+1229delinsTC
NM_147161.3:c.*184_*185delinsTC (ACOT11)	NP_671517.1:n.*184_*185delinsTC
NM_176782.2:c.1729_1730delinsGA (FAM151A)	NP_788954.2:p.Asp577=
XM_006710599.2:c.1651_1652delinsGA (FAM151A)	XP_006710662.1:p.Asp551=
XM_006710599.3:c.1651_1652delinsGA (FAM151A)	XP_006710662.1:p.Asp551=
NM_176782.3:c.1729_1730delinsGA (FAM151A) MANE Select	NP_788954.2:p.Asp577=
NM_015547.4:c.1629+1228_1629+1229delinsTC (ACOT11)	NP_056362.1:n.1629+1228_1629+1229delinsTC
NM_147161.4:c.*184_*185delinsTC (ACOT11) MANE Select	NP_671517.1:n.*184_*185delinsTC