Canonical Allele Identifier: CA1001886413

Gene: FAM151A ACOT11

Linked Data

• gnomAD v3: 1-54609221-T-TGAGCAGCTGTTCCCTGTAGCCACTGCCCAGCACCTCCTCAGGCCAGCCTGGTGCCACAGTCACGTGG
• gnomAD v4: 1-54609221-T-TGAGCAGCTGTTCCCTGTAGCCACTGCCCAGCACCTCCTCAGGCCAGCCTGGTGCCACAGTCACGTGG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.54609222_54609223insAGCAGCTGTTCCCTGTAGCCACTGCCCAGCACCTCCTCAGGCCAGCCTGGTGCCACAGTCACGTGGG , CM000663.2:g.54609222_54609223insAGCAGCTGTTCCCTGTAGCCACTGCCCAGCACCTCCTCAGGCCAGCCTGGTGCCACAGTCACGTGGG	GRCh38
NC_000001.10:g.55074895_55074896insAGCAGCTGTTCCCTGTAGCCACTGCCCAGCACCTCCTCAGGCCAGCCTGGTGCCACAGTCACGTGGG , CM000663.1:g.55074895_55074896insAGCAGCTGTTCCCTGTAGCCACTGCCCAGCACCTCCTCAGGCCAGCCTGGTGCCACAGTCACGTGGG	GRCh37
NC_000001.9:g.54847483_54847484insAGCAGCTGTTCCCTGTAGCCACTGCCCAGCACCTCCTCAGGCCAGCCTGGTGCCACAGTCACGTGGG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302250.7:c.*46_*47insCCACGTGACTGTGGCACCAGGCTGGCCTGAGGAGGTGCTGGGCAGTGGCTACAGGGAACAGCTGCTC (FAM151A) MANE Select	ENSP00000306888.2:n.*46_*47insCCACGTGACTGTGGCACCAGGCTGGCCTGAG...
ENST00000343744.7:c.*110_*111insAGCAGCTGTTCCCTGTAGCCACTGCCCAGCACCTCCTCAGGCCAGCCTGGTGCCACAGTCACGTGGG (ACOT11) MANE Select	ENSP00000340260.2:n.*110_*111insAGCAGCTGTTCCCTGTAGCCACTGCCCAG...
ENST00000302250.6:c.*46_*47insCCACGTGACTGTGGCACCAGGCTGGCCTGAGGAGGTGCTGGGCAGTGGCTACAGGGAACAGCTGCTC (FAM151A)	ENSP00000306888.2:n.*46_*47insCCACGTGACTGTGGCACCAGGCTGGCCTGAG...
ENST00000343744.6:c.*110_*111insAGCAGCTGTTCCCTGTAGCCACTGCCCAGCACCTCCTCAGGCCAGCCTGGTGCCACAGTCACGTGGG (ACOT11)	ENSP00000340260.2:n.*110_*111insAGCAGCTGTTCCCTGTAGCCACTGCCCAG...
ENST00000371304.2:c.*46_*47insCCACGTGACTGTGGCACCAGGCTGGCCTGAGGAGGTGCTGGGCAGTGGCTACAGGGAACAGCTGCTC (FAM151A)	ENSP00000360353.2:n.*46_*47insCCACGTGACTGTGGCACCAGGCTGGCCTGAG...
ENST00000371316.3:c.1629+1154_1629+1155insAGCAGCTGTTCCCTGTAGCCACTGCCCAGCACCTCCTCAGGCCAGCCTGGTGCCACAGTCACGTGGG (ACOT11)	ENSP00000360366.3:n.1629+1154_1629+1155insAGCAGCTGTTCCCTGTAGC...
ENST00000481208.5:n.1973_1974insAGCAGCTGTTCCCTGTAGCCACTGCCCAGCACCTCCTCAGGCCAGCCTGGTGCCACAGTCACGTGGG (ACOT11)
NM_015547.3:c.1629+1154_1629+1155insAGCAGCTGTTCCCTGTAGCCACTGCCCAGCACCTCCTCAGGCCAGCCTGGTGCCACAGTCACGTGGG (ACOT11)	NP_056362.1:n.1629+1154_1629+1155insAGCAGCTGTTCCCTGTAGCCACTGC...
NM_147161.3:c.*110_*111insAGCAGCTGTTCCCTGTAGCCACTGCCCAGCACCTCCTCAGGCCAGCCTGGTGCCACAGTCACGTGGG (ACOT11)	NP_671517.1:n.*110_*111insAGCAGCTGTTCCCTGTAGCCACTGCCCAGCACCTC...
NM_176782.2:c.*46_*47insCCACGTGACTGTGGCACCAGGCTGGCCTGAGGAGGTGCTGGGCAGTGGCTACAGGGAACAGCTGCTC (FAM151A)	NP_788954.2:n.*46_*47insCCACGTGACTGTGGCACCAGGCTGGCCTGAGGAGGTG...
XM_006710599.2:c.*46_*47insCCACGTGACTGTGGCACCAGGCTGGCCTGAGGAGGTGCTGGGCAGTGGCTACAGGGAACAGCTGCTC (FAM151A)	XP_006710662.1:n.*46_*47insCCACGTGACTGTGGCACCAGGCTGGCCTGAGGAG...
XM_006710599.3:c.*46_*47insCCACGTGACTGTGGCACCAGGCTGGCCTGAGGAGGTGCTGGGCAGTGGCTACAGGGAACAGCTGCTC (FAM151A)	XP_006710662.1:n.*46_*47insCCACGTGACTGTGGCACCAGGCTGGCCTGAGGAG...
NM_176782.3:c.*46_*47insCCACGTGACTGTGGCACCAGGCTGGCCTGAGGAGGTGCTGGGCAGTGGCTACAGGGAACAGCTGCTC (FAM151A) MANE Select	NP_788954.2:n.*46_*47insCCACGTGACTGTGGCACCAGGCTGGCCTGAGGAGGTG...
NM_015547.4:c.1629+1154_1629+1155insAGCAGCTGTTCCCTGTAGCCACTGCCCAGCACCTCCTCAGGCCAGCCTGGTGCCACAGTCACGTGGG (ACOT11)	NP_056362.1:n.1629+1154_1629+1155insAGCAGCTGTTCCCTGTAGCCACTGC...
NM_147161.4:c.*110_*111insAGCAGCTGTTCCCTGTAGCCACTGCCCAGCACCTCCTCAGGCCAGCCTGGTGCCACAGTCACGTGGG (ACOT11) MANE Select	NP_671517.1:n.*110_*111insAGCAGCTGTTCCCTGTAGCCACTGCCCAGCACCTC...