Canonical Allele Identifier: CA2645794422

Gene: FAM151A ACOT11

Linked Data

• gnomAD v4: 1-54609193-A-ACACAGGTATGGTGTAAATAAACCTGTGTTGCCATGGCAAC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.54609193_54609194insCACAGGTATGGTGTAAATAAACCTGTGTTGCCATGGCAAC , CM000663.2:g.54609193_54609194insCACAGGTATGGTGTAAATAAACCTGTGTTGCCATGGCAAC	GRCh38
NC_000001.10:g.55074866_55074867insCACAGGTATGGTGTAAATAAACCTGTGTTGCCATGGCAAC , CM000663.1:g.55074866_55074867insCACAGGTATGGTGTAAATAAACCTGTGTTGCCATGGCAAC	GRCh37
NC_000001.9:g.54847454_54847455insCACAGGTATGGTGTAAATAAACCTGTGTTGCCATGGCAAC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302250.7:c.*74_*75insGTTGCCATGGCAACACAGGTTTATTTACACCATACCTGTG (FAM151A) MANE Select	ENSP00000306888.2:n.*74_*75insGTTGCCATGGCAACACAGGTTTATTTACACC...
ENST00000343744.7:c.*81_*82insCACAGGTATGGTGTAAATAAACCTGTGTTGCCATGGCAAC (ACOT11) MANE Select	ENSP00000340260.2:n.*81_*82insCACAGGTATGGTGTAAATAAACCTGTGTTGC...
ENST00000302250.6:c.*74_*75insGTTGCCATGGCAACACAGGTTTATTTACACCATACCTGTG (FAM151A)	ENSP00000306888.2:n.*74_*75insGTTGCCATGGCAACACAGGTTTATTTACACC...
ENST00000343744.6:c.*81_*82insCACAGGTATGGTGTAAATAAACCTGTGTTGCCATGGCAAC (ACOT11)	ENSP00000340260.2:n.*81_*82insCACAGGTATGGTGTAAATAAACCTGTGTTGC...
ENST00000371304.2:c.*74_*75insGTTGCCATGGCAACACAGGTTTATTTACACCATACCTGTG (FAM151A)	ENSP00000360353.2:n.*74_*75insGTTGCCATGGCAACACAGGTTTATTTACACC...
ENST00000371316.3:c.1629+1125_1629+1126insCACAGGTATGGTGTAAATAAACCTGTGTTGCCATGGCAAC (ACOT11)	ENSP00000360366.3:n.1629+1125_1629+1126insCACAGGTATGGTGTAAATA...
ENST00000481208.5:n.1944_1945insCACAGGTATGGTGTAAATAAACCTGTGTTGCCATGGCAAC (ACOT11)
NM_015547.3:c.1629+1125_1629+1126insCACAGGTATGGTGTAAATAAACCTGTGTTGCCATGGCAAC (ACOT11)	NP_056362.1:n.1629+1125_1629+1126insCACAGGTATGGTGTAAATAAACCTG...
NM_147161.3:c.*81_*82insCACAGGTATGGTGTAAATAAACCTGTGTTGCCATGGCAAC (ACOT11)	NP_671517.1:n.*81_*82insCACAGGTATGGTGTAAATAAACCTGTGTTGCCATGGC...
NM_176782.2:c.*74_*75insGTTGCCATGGCAACACAGGTTTATTTACACCATACCTGTG (FAM151A)	NP_788954.2:n.*74_*75insGTTGCCATGGCAACACAGGTTTATTTACACCATACCT...
XM_006710599.2:c.*74_*75insGTTGCCATGGCAACACAGGTTTATTTACACCATACCTGTG (FAM151A)	XP_006710662.1:n.*74_*75insGTTGCCATGGCAACACAGGTTTATTTACACCATA...
XM_006710599.3:c.*74_*75insGTTGCCATGGCAACACAGGTTTATTTACACCATACCTGTG (FAM151A)	XP_006710662.1:n.*74_*75insGTTGCCATGGCAACACAGGTTTATTTACACCATA...
NM_176782.3:c.*74_*75insGTTGCCATGGCAACACAGGTTTATTTACACCATACCTGTG (FAM151A) MANE Select	NP_788954.2:n.*74_*75insGTTGCCATGGCAACACAGGTTTATTTACACCATACCT...
NM_015547.4:c.1629+1125_1629+1126insCACAGGTATGGTGTAAATAAACCTGTGTTGCCATGGCAAC (ACOT11)	NP_056362.1:n.1629+1125_1629+1126insCACAGGTATGGTGTAAATAAACCTG...
NM_147161.4:c.*81_*82insCACAGGTATGGTGTAAATAAACCTGTGTTGCCATGGCAAC (ACOT11) MANE Select	NP_671517.1:n.*81_*82insCACAGGTATGGTGTAAATAAACCTGTGTTGCCATGGC...