Canonical Allele Identifier: CA916179736
Gene: FAM151A HGNC NCBI
ACOT11 HGNC NCBI

Linked Data

dbSNP Id: rs1553165138

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.54609248_54609249insACCCACCACCCCGAGGTCCGCTG , CM000663.2:g.54609248_54609249insACCCACCACCCCGAGGTCCGCTG GRCh38
NC_000001.10:g.55074921_55074922insACCCACCACCCCGAGGTCCGCTG , CM000663.1:g.55074921_55074922insACCCACCACCCCGAGGTCCGCTG GRCh37
NC_000001.9:g.54847509_54847510insACCCACCACCCCGAGGTCCGCTG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000302250.7:c.*30_*31insGGGGTGGTGGGTCAGCGGACCTC (FAM151A) MANE Select ENSP00000306888.2:n.*30_*31insGGGGTGGTGGGTCAGCGGACCTC
ENST00000343744.7:c.*136_*137insACCCACCACCCCGAGGTCCGCTG (ACOT11) MANE Select ENSP00000340260.2:n.*136_*137insACCCACCACCCCGAGGTCCGCTG
ENST00000302250.6:c.*30_*31insGGGGTGGTGGGTCAGCGGACCTC (FAM151A) ENSP00000306888.2:n.*30_*31insGGGGTGGTGGGTCAGCGGACCTC
ENST00000343744.6:c.*136_*137insACCCACCACCCCGAGGTCCGCTG (ACOT11) ENSP00000340260.2:n.*136_*137insACCCACCACCCCGAGGTCCGCTG
ENST00000371304.2:c.*30_*31insGGGGTGGTGGGTCAGCGGACCTC (FAM151A) ENSP00000360353.2:n.*30_*31insGGGGTGGTGGGTCAGCGGACCTC
ENST00000371316.3:c.1629+1180_1629+1181insACCCACCACCCCGAGGTCCGCTG (ACOT11) ENSP00000360366.3:n.1629+1180_1629+1181insACCCACCACCCCGAGGTCC...
ENST00000481208.5:n.1999_2000insACCCACCACCCCGAGGTCCGCTG (ACOT11)
NM_015547.3:c.1629+1180_1629+1181insACCCACCACCCCGAGGTCCGCTG (ACOT11) NP_056362.1:n.1629+1180_1629+1181insACCCACCACCCCGAGGTCCGCTG
NM_147161.3:c.*136_*137insACCCACCACCCCGAGGTCCGCTG (ACOT11) NP_671517.1:n.*136_*137insACCCACCACCCCGAGGTCCGCTG
NM_176782.2:c.*30_*31insGGGGTGGTGGGTCAGCGGACCTC (FAM151A) NP_788954.2:n.*30_*31insGGGGTGGTGGGTCAGCGGACCTC
XM_006710599.2:c.*30_*31insGGGGTGGTGGGTCAGCGGACCTC (FAM151A) XP_006710662.1:n.*30_*31insGGGGTGGTGGGTCAGCGGACCTC
XM_006710599.3:c.*30_*31insGGGGTGGTGGGTCAGCGGACCTC (FAM151A) XP_006710662.1:n.*30_*31insGGGGTGGTGGGTCAGCGGACCTC
NM_176782.3:c.*30_*31insGGGGTGGTGGGTCAGCGGACCTC (FAM151A) MANE Select NP_788954.2:n.*30_*31insGGGGTGGTGGGTCAGCGGACCTC
NM_015547.4:c.1629+1180_1629+1181insACCCACCACCCCGAGGTCCGCTG (ACOT11) NP_056362.1:n.1629+1180_1629+1181insACCCACCACCCCGAGGTCCGCTG
NM_147161.4:c.*136_*137insACCCACCACCCCGAGGTCCGCTG (ACOT11) MANE Select NP_671517.1:n.*136_*137insACCCACCACCCCGAGGTCCGCTG