Canonical Allele Identifier: CA523274596

Gene: FAM151A ACOT11

Linked Data

• dbSNP Id: rs776895107
• gnomAD v2: 1-55074898-A-AGCAGCTGTTCCCTGTAGCCACTGCCCAGCACCTCCTCAGGCC
• MyVariant Identifiers: chr1:g.55074899_55074906delinsGCAGCTGTTCCCTGTAGCCACTGCCCAGCACCTCCTCAGGCCAGCCTCCG (hg19) ; chr1:g.54609226_54609233delinsGCAGCTGTTCCCTGTAGCCACTGCCCAGCACCTCCTCAGGCCAGCCTCCG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.54609225_54609226insGCAGCTGTTCCCTGTAGCCACTGCCCAGCACCTCCTCAGGCC , CM000663.2:g.54609225_54609226insGCAGCTGTTCCCTGTAGCCACTGCCCAGCACCTCCTCAGGCC	GRCh38
NC_000001.10:g.55074898_55074899insGCAGCTGTTCCCTGTAGCCACTGCCCAGCACCTCCTCAGGCC , CM000663.1:g.55074898_55074899insGCAGCTGTTCCCTGTAGCCACTGCCCAGCACCTCCTCAGGCC	GRCh37
NC_000001.9:g.54847486_54847487insGCAGCTGTTCCCTGTAGCCACTGCCCAGCACCTCCTCAGGCC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302250.7:c.*42_*43insGGCCTGAGGAGGTGCTGGGCAGTGGCTACAGGGAACAGCTGC (FAM151A) MANE Select	ENSP00000306888.2:n.*42_*43insGGCCTGAGGAGGTGCTGGGCAGTGGCTACAG...
ENST00000343744.7:c.*113_*114insGCAGCTGTTCCCTGTAGCCACTGCCCAGCACCTCCTCAGGCC (ACOT11) MANE Select	ENSP00000340260.2:n.*113_*114insGCAGCTGTTCCCTGTAGCCACTGCCCAGC...
ENST00000302250.6:c.*42_*43insGGCCTGAGGAGGTGCTGGGCAGTGGCTACAGGGAACAGCTGC (FAM151A)	ENSP00000306888.2:n.*42_*43insGGCCTGAGGAGGTGCTGGGCAGTGGCTACAG...
ENST00000343744.6:c.*113_*114insGCAGCTGTTCCCTGTAGCCACTGCCCAGCACCTCCTCAGGCC (ACOT11)	ENSP00000340260.2:n.*113_*114insGCAGCTGTTCCCTGTAGCCACTGCCCAGC...
ENST00000371304.2:c.*42_*43insGGCCTGAGGAGGTGCTGGGCAGTGGCTACAGGGAACAGCTGC (FAM151A)	ENSP00000360353.2:n.*42_*43insGGCCTGAGGAGGTGCTGGGCAGTGGCTACAG...
ENST00000371316.3:c.1629+1157_1629+1158insGCAGCTGTTCCCTGTAGCCACTGCCCAGCACCTCCTCAGGCC (ACOT11)	ENSP00000360366.3:n.1629+1157_1629+1158insGCAGCTGTTCCCTGTAGCC...
ENST00000481208.5:n.1976_1977insGCAGCTGTTCCCTGTAGCCACTGCCCAGCACCTCCTCAGGCC (ACOT11)
NM_015547.3:c.1629+1157_1629+1158insGCAGCTGTTCCCTGTAGCCACTGCCCAGCACCTCCTCAGGCC (ACOT11)	NP_056362.1:n.1629+1157_1629+1158insGCAGCTGTTCCCTGTAGCCACTGCC...
NM_147161.3:c.*113_*114insGCAGCTGTTCCCTGTAGCCACTGCCCAGCACCTCCTCAGGCC (ACOT11)	NP_671517.1:n.*113_*114insGCAGCTGTTCCCTGTAGCCACTGCCCAGCACCTCC...
NM_176782.2:c.*42_*43insGGCCTGAGGAGGTGCTGGGCAGTGGCTACAGGGAACAGCTGC (FAM151A)	NP_788954.2:n.*42_*43insGGCCTGAGGAGGTGCTGGGCAGTGGCTACAGGGAACA...
XM_006710599.2:c.*42_*43insGGCCTGAGGAGGTGCTGGGCAGTGGCTACAGGGAACAGCTGC (FAM151A)	XP_006710662.1:n.*42_*43insGGCCTGAGGAGGTGCTGGGCAGTGGCTACAGGGA...
XM_006710599.3:c.*42_*43insGGCCTGAGGAGGTGCTGGGCAGTGGCTACAGGGAACAGCTGC (FAM151A)	XP_006710662.1:n.*42_*43insGGCCTGAGGAGGTGCTGGGCAGTGGCTACAGGGA...
NM_176782.3:c.*42_*43insGGCCTGAGGAGGTGCTGGGCAGTGGCTACAGGGAACAGCTGC (FAM151A) MANE Select	NP_788954.2:n.*42_*43insGGCCTGAGGAGGTGCTGGGCAGTGGCTACAGGGAACA...
NM_015547.4:c.1629+1157_1629+1158insGCAGCTGTTCCCTGTAGCCACTGCCCAGCACCTCCTCAGGCC (ACOT11)	NP_056362.1:n.1629+1157_1629+1158insGCAGCTGTTCCCTGTAGCCACTGCC...
NM_147161.4:c.*113_*114insGCAGCTGTTCCCTGTAGCCACTGCCCAGCACCTCCTCAGGCC (ACOT11) MANE Select	NP_671517.1:n.*113_*114insGCAGCTGTTCCCTGTAGCCACTGCCCAGCACCTCC...