Canonical Allele Identifier: CA6263401
Community Standard Title: NM_000019.4(ACAT1):c.1189C>A (p.His397Asn)
Gene: ACAT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108147295C>A , CM000673.2:g.108147295C>A GRCh38
NC_000011.9:g.108018022C>A , CM000673.1:g.108018022C>A GRCh37
NC_000011.8:g.107523232C>A NCBI36
NG_009888.1:g.30765C>A
NG_009888.2:g.35591C>A

Transcript Alleles

HGVS Amino-acid Change
NM_000019.4:c.1189C>A MANE Select NP_000010.1:p.His397Asn
ENST00000265838.9:c.1189C>A MANE Select ENSP00000265838.4:p.His397Asn
NM_000019.3:c.1189C>A NP_000010.1:p.His397Asn
NM_001386677.1:c.1210C>A NP_001373606.1:p.His404Asn
NM_001386678.1:c.874C>A NP_001373607.1:p.His292Asn
NM_001386679.1:c.892C>A NP_001373608.1:p.His298Asn
NM_001386681.1:c.919C>A NP_001373610.1:p.His307Asn
NM_001386682.1:c.919C>A NP_001373611.1:p.His307Asn
NM_001386685.1:c.919C>A NP_001373614.1:p.His307Asn
NM_001386686.1:c.919C>A NP_001373615.1:p.His307Asn
NM_001386687.1:c.919C>A NP_001373616.1:p.His307Asn
NM_001386688.1:c.919C>A NP_001373617.1:p.His307Asn
NM_001386689.1:c.919C>A NP_001373618.1:p.His307Asn
NM_001386690.1:c.919C>A NP_001373619.1:p.His307Asn
NM_001386691.1:c.919C>A NP_001373620.1:p.His307Asn
NR_170162.1:n.1164C>A
NR_170163.1:n.1222C>A
ENST00000265838.8:c.1189C>A ENSP00000265838.4:p.His397Asn
ENST00000533597.1:n.265C>A
ENST00000671707.1:n.1284C>A
ENST00000672031.1:c.*176C>A ENSP00000500463.1:n.*176C>A
ENST00000672284.1:c.919C>A ENSP00000500444.1:p.His307Asn
ENST00000672354.1:c.1210C>A ENSP00000500490.1:p.His404Asn
ENST00000672367.1:c.826C>A ENSP00000500209.1:p.His276Asn
ENST00000672580.1:c.*444C>A ENSP00000500366.1:n.*444C>A
ENST00000672907.1:c.874C>A ENSP00000500928.1:p.His292Asn
ENST00000673000.1:n.1277C>A
ENST00000673531.1:c.919C>A ENSP00000500163.1:p.His307Asn
XM_006718834.2:c.919C>A XP_006718897.1:p.His307Asn
XM_006718835.2:c.919C>A XP_006718898.1:p.His307Asn
XM_006718835.3:c.919C>A XP_006718898.1:p.His307Asn
XM_017017681.1:c.919C>A XP_016873170.1:p.His307Asn
XM_017017682.2:c.811C>A XP_016873171.1:p.His271Asn
XM_017017683.2:c.811C>A XP_016873172.1:p.His271Asn
XM_024448511.1:c.919C>A XP_024304279.1:p.His307Asn
XM_024448512.1:c.919C>A XP_024304280.1:p.His307Asn
XM_024448513.1:c.919C>A XP_024304281.1:p.His307Asn
XM_024448514.1:c.919C>A XP_024304282.1:p.His307Asn
XM_024448515.1:c.919C>A XP_024304283.1:p.His307Asn