Canonical Allele Identifier: CA1998721169
Gene: ACAT1 HGNC NCBI

Linked Data

dbSNP Id: rs2077748326

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108147618dup , CM000673.2:g.108147618dup GRCh38
NC_000011.9:g.108018345dup , CM000673.1:g.108018345dup GRCh37
NC_000011.8:g.107523555dup NCBI36
NG_009888.1:g.31088dup
NG_009888.2:g.35914dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000265838.8:c.*228dup ENSP00000265838.4:n.*228dup
NM_000019.3:c.*228dup NP_000010.1:n.*228dup
XM_006718834.2:c.*228dup XP_006718897.1:n.*228dup
XM_006718835.2:c.*228dup XP_006718898.1:n.*228dup
XM_017017682.2:c.*228dup XP_016873171.1:n.*228dup
XM_017017683.2:c.*228dup XP_016873172.1:n.*228dup