Canonical Allele Identifier: CA1167798422

Gene: FAM151A ACOT11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.54609301_54609302delinsGT , CM000663.2:g.54609301_54609302delinsGT	GRCh38
NC_000001.10:g.55074974_55074975delinsGT , CM000663.1:g.55074974_55074975delinsGT	GRCh37
NC_000001.9:g.54847562_54847563delinsGT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302250.7:c.1724_1725delinsAC (FAM151A) MANE Select	ENSP00000306888.2:p.His575=
ENST00000343744.7:c.*189_*190delinsGT (ACOT11) MANE Select	ENSP00000340260.2:n.*189_*190delinsGT
ENST00000302250.6:c.1724_1725delinsAC (FAM151A)	ENSP00000306888.2:p.His575=
ENST00000343744.6:c.*189_*190delinsGT (ACOT11)	ENSP00000340260.2:n.*189_*190delinsGT
ENST00000371304.2:c.1163_1164delinsAC (FAM151A)	ENSP00000360353.2:p.His388=
ENST00000371316.3:c.1629+1233_1629+1234delinsGT (ACOT11)	ENSP00000360366.3:n.1629+1233_1629+1234delinsGT
ENST00000481208.5:n.2052_2053delinsGT (ACOT11)
NM_015547.3:c.1629+1233_1629+1234delinsGT (ACOT11)	NP_056362.1:n.1629+1233_1629+1234delinsGT
NM_147161.3:c.*189_*190delinsGT (ACOT11)	NP_671517.1:n.*189_*190delinsGT
NM_176782.2:c.1724_1725delinsAC (FAM151A)	NP_788954.2:p.His575=
XM_006710599.2:c.1646_1647delinsAC (FAM151A)	XP_006710662.1:p.His549=
XM_006710599.3:c.1646_1647delinsAC (FAM151A)	XP_006710662.1:p.His549=
NM_176782.3:c.1724_1725delinsAC (FAM151A) MANE Select	NP_788954.2:p.His575=
NM_015547.4:c.1629+1233_1629+1234delinsGT (ACOT11)	NP_056362.1:n.1629+1233_1629+1234delinsGT
NM_147161.4:c.*189_*190delinsGT (ACOT11) MANE Select	NP_671517.1:n.*189_*190delinsGT