Canonical Allele Identifier: CA671406811
Gene: ACAT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108133833dup , CM000673.2:g.108133833dup GRCh38
NC_000011.9:g.108004560dup , CM000673.1:g.108004560dup GRCh37
NC_000011.8:g.107509770dup NCBI36
NG_009888.1:g.17303dup
NG_009888.2:g.22129dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000265838.9:c.134dup MANE Select ENSP00000265838.4:p.Ser46LysfsTer21
ENST00000671707.1:n.229dup
ENST00000672008.1:c.134dup ENSP00000500499.1:p.Ser46LysfsTer21
ENST00000672031.1:c.134dup ENSP00000500463.1:p.Ser46LysfsTer21
ENST00000672284.1:c.-137dup ENSP00000500444.1:n.-137dup
ENST00000672354.1:c.134dup ENSP00000500490.1:p.Ser46LysfsTer21
ENST00000672367.1:c.73-5065dup ENSP00000500209.1:n.73-5065dup
ENST00000672580.1:c.134dup ENSP00000500366.1:p.Ser46LysfsTer21
ENST00000672907.1:c.120+1879dup ENSP00000500928.1:n.120+1879dup
ENST00000673000.1:n.222dup
ENST00000673531.1:c.-137dup ENSP00000500163.1:n.-137dup
ENST00000265838.8:c.134dup ENSP00000265838.4:p.Ser46LysfsTer21
ENST00000299355.10:c.134dup ENSP00000299355.6:p.Ser46LysfsTer21
ENST00000524833.5:n.174dup
ENST00000527942.5:c.-137dup ENSP00000433568.1:n.-137dup
ENST00000531813.5:c.134dup ENSP00000435965.1:p.Ser46LysfsTer21
ENST00000531853.5:n.398dup
NM_000019.3:c.134dup NP_000010.1:p.Ser46LysfsTer21
XM_006718834.2:c.-137dup XP_006718897.1:n.-137dup
XM_006718835.2:c.-137dup XP_006718898.1:n.-137dup
XM_006718835.3:c.-137dup XP_006718898.1:n.-137dup
XM_017017681.1:c.-137dup XP_016873170.1:n.-137dup
XM_017017682.2:c.-144dup XP_016873171.1:n.-144dup
XM_017017683.2:c.-144dup XP_016873172.1:n.-144dup
XM_024448511.1:c.-137dup XP_024304279.1:n.-137dup
XM_024448512.1:c.-137dup XP_024304280.1:n.-137dup
XM_024448513.1:c.-137dup XP_024304281.1:n.-137dup
XM_024448514.1:c.-137dup XP_024304282.1:n.-137dup
XM_024448515.1:c.-137dup XP_024304283.1:n.-137dup
NM_000019.4:c.134dup MANE Select NP_000010.1:p.Ser46LysfsTer21
NM_001386677.1:c.134dup NP_001373606.1:p.Ser46LysfsTer21
NM_001386678.1:c.120+1879dup NP_001373607.1:n.120+1879dup
NM_001386679.1:c.-144dup NP_001373608.1:n.-144dup
NM_001386681.1:c.-137dup NP_001373610.1:n.-137dup
NM_001386682.1:c.-137dup NP_001373611.1:n.-137dup
NM_001386685.1:c.-137dup NP_001373614.1:n.-137dup
NM_001386686.1:c.-137dup NP_001373615.1:n.-137dup
NM_001386687.1:c.-137dup NP_001373616.1:n.-137dup
NM_001386688.1:c.-137dup NP_001373617.1:n.-137dup
NM_001386689.1:c.-137dup NP_001373618.1:n.-137dup
NM_001386690.1:c.-137dup NP_001373619.1:n.-137dup
NM_001386691.1:c.-137dup NP_001373620.1:n.-137dup
NR_170162.1:n.174dup
NR_170163.1:n.268dup