Canonical Allele Identifier: CA2645794468

Gene: FAM151A ACOT11

Linked Data

• gnomAD v4: 1-54609686-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.54609690del , CM000663.2:g.54609690del	GRCh38
NC_000001.10:g.55075363del , CM000663.1:g.55075363del	GRCh37
NC_000001.9:g.54847951del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302250.7:c.1339del (FAM151A) MANE Select	ENSP00000306888.2:p.Ile447SerfsTer28
ENST00000343744.7:c.*578del (ACOT11) MANE Select	ENSP00000340260.2:n.*578del
ENST00000302250.6:c.1339del (FAM151A)	ENSP00000306888.2:p.Ile447SerfsTer28
ENST00000343744.6:c.*578del (ACOT11)	ENSP00000340260.2:n.*578del
ENST00000371304.2:c.918-140del (FAM151A)	ENSP00000360353.2:n.918-140del
ENST00000371316.3:c.1629+1622del (ACOT11)	ENSP00000360366.3:n.1629+1622del
ENST00000481208.5:n.2441del (ACOT11)
NM_015547.3:c.1629+1622del (ACOT11)	NP_056362.1:n.1629+1622del
NM_147161.3:c.*578del (ACOT11)	NP_671517.1:n.*578del
NM_176782.2:c.1339del (FAM151A)	NP_788954.2:p.Ile447SerfsTer28
XM_006710599.2:c.1261del (FAM151A)	XP_006710662.1:p.Ile421SerfsTer28
XM_006710599.3:c.1261del (FAM151A)	XP_006710662.1:p.Ile421SerfsTer28
NM_176782.3:c.1339del (FAM151A) MANE Select	NP_788954.2:p.Ile447SerfsTer28
NM_015547.4:c.1629+1622del (ACOT11)	NP_056362.1:n.1629+1622del
NM_147161.4:c.*578del (ACOT11) MANE Select	NP_671517.1:n.*578del