Canonical Allele Identifier: CA2574378784

Gene: FAM151A ACOT11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.54609678del , CM000663.2:g.54609678del	GRCh38
NC_000001.10:g.55075351del , CM000663.1:g.55075351del	GRCh37
NC_000001.9:g.54847939del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302250.7:c.1350del (FAM151A) MANE Select	ENSP00000306888.2:p.Ser451ValfsTer24
ENST00000343744.7:c.*566del (ACOT11) MANE Select	ENSP00000340260.2:n.*566del
ENST00000302250.6:c.1350del (FAM151A)	ENSP00000306888.2:p.Ser451ValfsTer24
ENST00000343744.6:c.*566del (ACOT11)	ENSP00000340260.2:n.*566del
ENST00000371304.2:c.918-129del (FAM151A)	ENSP00000360353.2:n.918-129del
ENST00000371316.3:c.1629+1610del (ACOT11)	ENSP00000360366.3:n.1629+1610del
ENST00000481208.5:n.2429del (ACOT11)
NM_015547.3:c.1629+1610del (ACOT11)	NP_056362.1:n.1629+1610del
NM_147161.3:c.*566del (ACOT11)	NP_671517.1:n.*566del
NM_176782.2:c.1350del (FAM151A)	NP_788954.2:p.Ser451ValfsTer24
XM_006710599.2:c.1272del (FAM151A)	XP_006710662.1:p.Ser425ValfsTer24
XM_006710599.3:c.1272del (FAM151A)	XP_006710662.1:p.Ser425ValfsTer24
NM_176782.3:c.1350del (FAM151A) MANE Select	NP_788954.2:p.Ser451ValfsTer24
NM_015547.4:c.1629+1610del (ACOT11)	NP_056362.1:n.1629+1610del
NM_147161.4:c.*566del (ACOT11) MANE Select	NP_671517.1:n.*566del