Canonical Allele Identifier: CA523274604

Gene: FAM151A ACOT11

Linked Data

• dbSNP Id: rs1557667502
• gnomAD v2: 1-55074922-G-GGGAAGCCTCCGCCCTGAGGTCCGCTGA
• gnomAD v4: 1-54609249-G-GGGAAGCCTCCGCCCTGAGGTCCGCTGA
• MyVariant Identifiers: chr1:g.55074922_55074923insGGAAGCCTCCGCCCTGAGGTCCGCTGA (hg19) ; chr1:g.54609249_54609250insGGAAGCCTCCGCCCTGAGGTCCGCTGA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.54609249_54609250insGGAAGCCTCCGCCCTGAGGTCCGCTGA , CM000663.2:g.54609249_54609250insGGAAGCCTCCGCCCTGAGGTCCGCTGA	GRCh38
NC_000001.10:g.55074922_55074923insGGAAGCCTCCGCCCTGAGGTCCGCTGA , CM000663.1:g.55074922_55074923insGGAAGCCTCCGCCCTGAGGTCCGCTGA	GRCh37
NC_000001.9:g.54847510_54847511insGGAAGCCTCCGCCCTGAGGTCCGCTGA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302250.7:c.*18_*19insTCAGCGGACCTCAGGGCGGAGGCTTCC (FAM151A) MANE Select	ENSP00000306888.2:n.*18_*19insTCAGCGGACCTCAGGGCGGAGGCTTCC
ENST00000343744.7:c.*137_*138insGGAAGCCTCCGCCCTGAGGTCCGCTGA (ACOT11) MANE Select	ENSP00000340260.2:n.*137_*138insGGAAGCCTCCGCCCTGAGGTCCGCTGA
ENST00000302250.6:c.*18_*19insTCAGCGGACCTCAGGGCGGAGGCTTCC (FAM151A)	ENSP00000306888.2:n.*18_*19insTCAGCGGACCTCAGGGCGGAGGCTTCC
ENST00000343744.6:c.*137_*138insGGAAGCCTCCGCCCTGAGGTCCGCTGA (ACOT11)	ENSP00000340260.2:n.*137_*138insGGAAGCCTCCGCCCTGAGGTCCGCTGA
ENST00000371304.2:c.*18_*19insTCAGCGGACCTCAGGGCGGAGGCTTCC (FAM151A)	ENSP00000360353.2:n.*18_*19insTCAGCGGACCTCAGGGCGGAGGCTTCC
ENST00000371316.3:c.1629+1181_1629+1182insGGAAGCCTCCGCCCTGAGGTCCGCTGA (ACOT11)	ENSP00000360366.3:n.1629+1181_1629+1182insGGAAGCCTCCGCCCTGAGG...
ENST00000481208.5:n.2000_2001insGGAAGCCTCCGCCCTGAGGTCCGCTGA (ACOT11)
NM_015547.3:c.1629+1181_1629+1182insGGAAGCCTCCGCCCTGAGGTCCGCTGA (ACOT11)	NP_056362.1:n.1629+1181_1629+1182insGGAAGCCTCCGCCCTGAGGTCCGCT...
NM_147161.3:c.*137_*138insGGAAGCCTCCGCCCTGAGGTCCGCTGA (ACOT11)	NP_671517.1:n.*137_*138insGGAAGCCTCCGCCCTGAGGTCCGCTGA
NM_176782.2:c.*18_*19insTCAGCGGACCTCAGGGCGGAGGCTTCC (FAM151A)	NP_788954.2:n.*18_*19insTCAGCGGACCTCAGGGCGGAGGCTTCC
XM_006710599.2:c.*18_*19insTCAGCGGACCTCAGGGCGGAGGCTTCC (FAM151A)	XP_006710662.1:n.*18_*19insTCAGCGGACCTCAGGGCGGAGGCTTCC
XM_006710599.3:c.*18_*19insTCAGCGGACCTCAGGGCGGAGGCTTCC (FAM151A)	XP_006710662.1:n.*18_*19insTCAGCGGACCTCAGGGCGGAGGCTTCC
NM_176782.3:c.*18_*19insTCAGCGGACCTCAGGGCGGAGGCTTCC (FAM151A) MANE Select	NP_788954.2:n.*18_*19insTCAGCGGACCTCAGGGCGGAGGCTTCC
NM_015547.4:c.1629+1181_1629+1182insGGAAGCCTCCGCCCTGAGGTCCGCTGA (ACOT11)	NP_056362.1:n.1629+1181_1629+1182insGGAAGCCTCCGCCCTGAGGTCCGCT...
NM_147161.4:c.*137_*138insGGAAGCCTCCGCCCTGAGGTCCGCTGA (ACOT11) MANE Select	NP_671517.1:n.*137_*138insGGAAGCCTCCGCCCTGAGGTCCGCTGA