Canonical Allele Identifier: CA1167798349

Gene: FAM151A ACOT11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.54609191_54609193delinsCAA , CM000663.2:g.54609191_54609193delinsCAA	GRCh38
NC_000001.10:g.55074864_55074866delinsCAA , CM000663.1:g.55074864_55074866delinsCAA	GRCh37
NC_000001.9:g.54847452_54847454delinsCAA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302250.7:c.*75_*77delinsTTG (FAM151A) MANE Select	ENSP00000306888.2:n.*75_*77delinsTTG
ENST00000343744.7:c.*79_*81delinsCAA (ACOT11) MANE Select	ENSP00000340260.2:n.*79_*81delinsCAA
ENST00000302250.6:c.*75_*77delinsTTG (FAM151A)	ENSP00000306888.2:n.*75_*77delinsTTG
ENST00000343744.6:c.*79_*81delinsCAA (ACOT11)	ENSP00000340260.2:n.*79_*81delinsCAA
ENST00000371304.2:c.*75_*77delinsTTG (FAM151A)	ENSP00000360353.2:n.*75_*77delinsTTG
ENST00000371316.3:c.1629+1123_1629+1125delinsCAA (ACOT11)	ENSP00000360366.3:n.1629+1123_1629+1125delinsCAA
ENST00000481208.5:n.1942_1944delinsCAA (ACOT11)
NM_015547.3:c.1629+1123_1629+1125delinsCAA (ACOT11)	NP_056362.1:n.1629+1123_1629+1125delinsCAA
NM_147161.3:c.*79_*81delinsCAA (ACOT11)	NP_671517.1:n.*79_*81delinsCAA
NM_176782.2:c.*75_*77delinsTTG (FAM151A)	NP_788954.2:n.*75_*77delinsTTG
XM_006710599.2:c.*75_*77delinsTTG (FAM151A)	XP_006710662.1:n.*75_*77delinsTTG
XM_006710599.3:c.*75_*77delinsTTG (FAM151A)	XP_006710662.1:n.*75_*77delinsTTG
NM_176782.3:c.*75_*77delinsTTG (FAM151A) MANE Select	NP_788954.2:n.*75_*77delinsTTG
NM_015547.4:c.1629+1123_1629+1125delinsCAA (ACOT11)	NP_056362.1:n.1629+1123_1629+1125delinsCAA
NM_147161.4:c.*79_*81delinsCAA (ACOT11) MANE Select	NP_671517.1:n.*79_*81delinsCAA