Canonical Allele Identifier: CA382508692
Gene: ACAT1 HGNC NCBI

Linked Data

dbSNP Id: rs1234025676

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108147271A>G , CM000673.2:g.108147271A>G GRCh38
NC_000011.9:g.108017998A>G , CM000673.1:g.108017998A>G GRCh37
NC_000011.8:g.107523208A>G NCBI36
NG_009888.1:g.30741A>G
NG_009888.2:g.35567A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000265838.9:c.1165A>G MANE Select ENSP00000265838.4:p.Met389Val
ENST00000671707.1:n.1260A>G
ENST00000672031.1:c.*152A>G ENSP00000500463.1:n.*152A>G
ENST00000672284.1:c.895A>G ENSP00000500444.1:p.Met299Val
ENST00000672354.1:c.1186A>G ENSP00000500490.1:p.Met396Val
ENST00000672367.1:c.802A>G ENSP00000500209.1:p.Met268Val
ENST00000672580.1:c.*420A>G ENSP00000500366.1:n.*420A>G
ENST00000672907.1:c.850A>G ENSP00000500928.1:p.Met284Val
ENST00000673000.1:n.1253A>G
ENST00000673531.1:c.895A>G ENSP00000500163.1:p.Met299Val
ENST00000265838.8:c.1165A>G ENSP00000265838.4:p.Met389Val
ENST00000533597.1:n.241A>G
NM_000019.3:c.1165A>G NP_000010.1:p.Met389Val
XM_006718834.2:c.895A>G XP_006718897.1:p.Met299Val
XM_006718835.2:c.895A>G XP_006718898.1:p.Met299Val
XM_006718835.3:c.895A>G XP_006718898.1:p.Met299Val
XM_017017681.1:c.895A>G XP_016873170.1:p.Met299Val
XM_017017682.2:c.787A>G XP_016873171.1:p.Met263Val
XM_017017683.2:c.787A>G XP_016873172.1:p.Met263Val
XM_024448511.1:c.895A>G XP_024304279.1:p.Met299Val
XM_024448512.1:c.895A>G XP_024304280.1:p.Met299Val
XM_024448513.1:c.895A>G XP_024304281.1:p.Met299Val
XM_024448514.1:c.895A>G XP_024304282.1:p.Met299Val
XM_024448515.1:c.895A>G XP_024304283.1:p.Met299Val
NM_000019.4:c.1165A>G MANE Select NP_000010.1:p.Met389Val
NM_001386677.1:c.1186A>G NP_001373606.1:p.Met396Val
NM_001386678.1:c.850A>G NP_001373607.1:p.Met284Val
NM_001386679.1:c.868A>G NP_001373608.1:p.Met290Val
NM_001386681.1:c.895A>G NP_001373610.1:p.Met299Val
NM_001386682.1:c.895A>G NP_001373611.1:p.Met299Val
NM_001386685.1:c.895A>G NP_001373614.1:p.Met299Val
NM_001386686.1:c.895A>G NP_001373615.1:p.Met299Val
NM_001386687.1:c.895A>G NP_001373616.1:p.Met299Val
NM_001386688.1:c.895A>G NP_001373617.1:p.Met299Val
NM_001386689.1:c.895A>G NP_001373618.1:p.Met299Val
NM_001386690.1:c.895A>G NP_001373619.1:p.Met299Val
NM_001386691.1:c.895A>G NP_001373620.1:p.Met299Val
NR_170162.1:n.1140A>G
NR_170163.1:n.1198A>G