Canonical Allele Identifier: CA15678029

Gene: ACAT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108144222A>C , CM000673.2:g.108144222A>C	GRCh38
NC_000011.9:g.108014949A>C , CM000673.1:g.108014949A>C	GRCh37
NC_000011.8:g.107520159A>C	NCBI36
NG_009888.1:g.27692A>C
NG_009888.2:g.32518A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000019.4:c.1005+175A>C MANE Select	NP_000010.1:n.1005+175A>C
ENST00000265838.9:c.1005+175A>C MANE Select	ENSP00000265838.4:n.1005+175A>C
NM_000019.3:c.1005+175A>C	NP_000010.1:n.1005+175A>C
NM_001386677.1:c.1005+175A>C	NP_001373606.1:n.1005+175A>C
NM_001386678.1:c.690+175A>C	NP_001373607.1:n.690+175A>C
NM_001386679.1:c.708+175A>C	NP_001373608.1:n.708+175A>C
NM_001386681.1:c.735+175A>C	NP_001373610.1:n.735+175A>C
NM_001386682.1:c.735+175A>C	NP_001373611.1:n.735+175A>C
NM_001386685.1:c.735+175A>C	NP_001373614.1:n.735+175A>C
NM_001386686.1:c.735+175A>C	NP_001373615.1:n.735+175A>C
NM_001386687.1:c.735+175A>C	NP_001373616.1:n.735+175A>C
NM_001386688.1:c.735+175A>C	NP_001373617.1:n.735+175A>C
NM_001386689.1:c.735+175A>C	NP_001373618.1:n.735+175A>C
NM_001386690.1:c.735+175A>C	NP_001373619.1:n.735+175A>C
NM_001386691.1:c.735+175A>C	NP_001373620.1:n.735+175A>C
NR_170162.1:n.980+1672A>C
NR_170163.1:n.1038+175A>C
ENST00000265838.8:c.1005+175A>C	ENSP00000265838.4:n.1005+175A>C
ENST00000671707.1:n.1100+175A>C
ENST00000672031.1:c.940+1672A>C	ENSP00000500463.1:n.940+1672A>C
ENST00000672284.1:c.735+175A>C	ENSP00000500444.1:n.735+175A>C
ENST00000672354.1:c.1005+175A>C	ENSP00000500490.1:n.1005+175A>C
ENST00000672367.1:c.642+175A>C	ENSP00000500209.1:n.642+175A>C
ENST00000672580.1:c.*260+175A>C	ENSP00000500366.1:n.*260+175A>C
ENST00000672907.1:c.690+175A>C	ENSP00000500928.1:n.690+175A>C
ENST00000673000.1:n.1093+175A>C
ENST00000673531.1:c.735+175A>C	ENSP00000500163.1:n.735+175A>C
XM_006718834.2:c.735+175A>C	XP_006718897.1:n.735+175A>C
XM_006718835.2:c.735+175A>C	XP_006718898.1:n.735+175A>C
XM_006718835.3:c.735+175A>C	XP_006718898.1:n.735+175A>C
XM_017017681.1:c.735+175A>C	XP_016873170.1:n.735+175A>C
XM_017017682.2:c.627+175A>C	XP_016873171.1:n.627+175A>C
XM_017017683.2:c.627+175A>C	XP_016873172.1:n.627+175A>C
XM_024448511.1:c.735+175A>C	XP_024304279.1:n.735+175A>C
XM_024448512.1:c.735+175A>C	XP_024304280.1:n.735+175A>C
XM_024448513.1:c.735+175A>C	XP_024304281.1:n.735+175A>C
XM_024448514.1:c.735+175A>C	XP_024304282.1:n.735+175A>C
XM_024448515.1:c.735+175A>C	XP_024304283.1:n.735+175A>C