Canonical Allele Identifier: CA1998716934

Gene: ACAT1

Linked Data

• dbSNP Id: rs2077520872
• gnomAD v4: 11-108138728-TTTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108138731_108138733del , CM000673.2:g.108138731_108138733del	GRCh38
NC_000011.9:g.108009458_108009460del , CM000673.1:g.108009458_108009460del	GRCh37
NC_000011.8:g.107514668_107514670del	NCBI36
NG_009888.1:g.22201_22203del
NG_009888.2:g.27027_27029del

Transcript Alleles

HGVS	Amino-acid change
ENST00000265838.9:c.436-167_436-165del MANE Select	ENSP00000265838.4:n.436-167_436-165del
ENST00000671707.1:n.531-167_531-165del
ENST00000672008.1:c.315-167_315-165del	ENSP00000500499.1:n.315-167_315-165del
ENST00000672031.1:c.436-167_436-165del	ENSP00000500463.1:n.436-167_436-165del
ENST00000672284.1:c.166-167_166-165del	ENSP00000500444.1:n.166-167_166-165del
ENST00000672354.1:c.436-167_436-165del	ENSP00000500490.1:n.436-167_436-165del
ENST00000672367.1:c.73-167_73-165del	ENSP00000500209.1:n.73-167_73-165del
ENST00000672580.1:c.436-167_436-165del	ENSP00000500366.1:n.436-167_436-165del
ENST00000672907.1:c.121-167_121-165del	ENSP00000500928.1:n.121-167_121-165del
ENST00000673000.1:n.524-167_524-165del
ENST00000673531.1:c.166-167_166-165del	ENSP00000500163.1:n.166-167_166-165del
ENST00000265838.8:c.436-167_436-165del	ENSP00000265838.4:n.436-167_436-165del
ENST00000528370.1:c.242-167_242-165del
ENST00000531813.5:c.335-167_335-165del	ENSP00000435965.1:n.335-167_335-165del
ENST00000534773.1:n.12_14del
NM_000019.3:c.436-167_436-165del	NP_000010.1:n.436-167_436-165del
XM_006718834.2:c.166-167_166-165del	XP_006718897.1:n.166-167_166-165del
XM_006718835.2:c.166-167_166-165del	XP_006718898.1:n.166-167_166-165del
XM_006718835.3:c.166-167_166-165del	XP_006718898.1:n.166-167_166-165del
XM_017017681.1:c.166-167_166-165del	XP_016873170.1:n.166-167_166-165del
XM_017017682.2:c.58-167_58-165del	XP_016873171.1:n.58-167_58-165del
XM_017017683.2:c.58-167_58-165del	XP_016873172.1:n.58-167_58-165del
XM_024448511.1:c.166-167_166-165del	XP_024304279.1:n.166-167_166-165del
XM_024448512.1:c.166-167_166-165del	XP_024304280.1:n.166-167_166-165del
XM_024448513.1:c.166-167_166-165del	XP_024304281.1:n.166-167_166-165del
XM_024448514.1:c.166-167_166-165del	XP_024304282.1:n.166-167_166-165del
XM_024448515.1:c.166-167_166-165del	XP_024304283.1:n.166-167_166-165del
NM_000019.4:c.436-167_436-165del MANE Select	NP_000010.1:n.436-167_436-165del
NM_001386677.1:c.436-167_436-165del	NP_001373606.1:n.436-167_436-165del
NM_001386678.1:c.121-167_121-165del	NP_001373607.1:n.121-167_121-165del
NM_001386679.1:c.139-167_139-165del	NP_001373608.1:n.139-167_139-165del
NM_001386681.1:c.166-167_166-165del	NP_001373610.1:n.166-167_166-165del
NM_001386682.1:c.166-167_166-165del	NP_001373611.1:n.166-167_166-165del
NM_001386685.1:c.166-167_166-165del	NP_001373614.1:n.166-167_166-165del
NM_001386686.1:c.166-167_166-165del	NP_001373615.1:n.166-167_166-165del
NM_001386687.1:c.166-167_166-165del	NP_001373616.1:n.166-167_166-165del
NM_001386688.1:c.166-167_166-165del	NP_001373617.1:n.166-167_166-165del
NM_001386689.1:c.166-167_166-165del	NP_001373618.1:n.166-167_166-165del
NM_001386690.1:c.166-167_166-165del	NP_001373619.1:n.166-167_166-165del
NM_001386691.1:c.166-167_166-165del	NP_001373620.1:n.166-167_166-165del
NR_170162.1:n.476-167_476-165del
NR_170163.1:n.469-167_469-165del