Canonical Allele Identifier: CA10629775
Gene: ACAT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 302230
ClinVar RCV Id: RCV000399149
dbSNP Id: rs886047605

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108148065A>C , CM000673.2:g.108148065A>C GRCh38
NC_000011.9:g.108018792A>C , CM000673.1:g.108018792A>C GRCh37
NC_000011.8:g.107524002A>C NCBI36
NG_009888.1:g.31535A>C
NG_009888.2:g.36361A>C

Transcript Alleles

HGVS Amino-acid Change
NM_000019.3:c.*675A>C NP_000010.1:n.*675A>C
XM_006718834.2:c.*675A>C XP_006718897.1:n.*675A>C
XM_006718835.2:c.*675A>C XP_006718898.1:n.*675A>C
XM_017017682.2:c.*675A>C XP_016873171.1:n.*675A>C
XM_017017683.2:c.*675A>C XP_016873172.1:n.*675A>C