Canonical Allele Identifier: CA2615844509

Gene: ACAT1

Linked Data

• ClinVar Variation Id: 2776684
• ClinVar RCV Id: RCV003605888
• gnomAD v4: 11-108146374-TAAC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108146375_108146377del , CM000673.2:g.108146375_108146377del	GRCh38
NC_000011.9:g.108017102_108017104del , CM000673.1:g.108017102_108017104del	GRCh37
NC_000011.8:g.107522312_107522314del	NCBI36
NG_009888.1:g.29845_29847del
NG_009888.2:g.34671_34673del

Transcript Alleles

HGVS	Amino-acid change
ENST00000265838.9:c.1163+16_1163+18del MANE Select	ENSP00000265838.4:n.1163+16_1163+18del
ENST00000671707.1:n.1258+16_1258+18del
ENST00000672031.1:c.*150+16_*150+18del	ENSP00000500463.1:n.*150+16_*150+18del
ENST00000672284.1:c.893+16_893+18del	ENSP00000500444.1:n.893+16_893+18del
ENST00000672354.1:c.1163+16_1163+18del	ENSP00000500490.1:n.1163+16_1163+18del
ENST00000672367.1:c.800+16_800+18del	ENSP00000500209.1:n.800+16_800+18del
ENST00000672580.1:c.*418+16_*418+18del	ENSP00000500366.1:n.*418+16_*418+18del
ENST00000672907.1:c.848+16_848+18del	ENSP00000500928.1:n.848+16_848+18del
ENST00000673000.1:n.1251+16_1251+18del
ENST00000673531.1:c.893+16_893+18del	ENSP00000500163.1:n.893+16_893+18del
ENST00000265838.8:c.1163+16_1163+18del	ENSP00000265838.4:n.1163+16_1163+18del
ENST00000533597.1:n.239+16_239+18del
NM_000019.3:c.1163+16_1163+18del	NP_000010.1:n.1163+16_1163+18del
XM_006718834.2:c.893+16_893+18del	XP_006718897.1:n.893+16_893+18del
XM_006718835.2:c.893+16_893+18del	XP_006718898.1:n.893+16_893+18del
XM_006718835.3:c.893+16_893+18del	XP_006718898.1:n.893+16_893+18del
XM_017017681.1:c.893+16_893+18del	XP_016873170.1:n.893+16_893+18del
XM_017017682.2:c.785+16_785+18del	XP_016873171.1:n.785+16_785+18del
XM_017017683.2:c.785+16_785+18del	XP_016873172.1:n.785+16_785+18del
XM_024448511.1:c.893+16_893+18del	XP_024304279.1:n.893+16_893+18del
XM_024448512.1:c.893+16_893+18del	XP_024304280.1:n.893+16_893+18del
XM_024448513.1:c.893+16_893+18del	XP_024304281.1:n.893+16_893+18del
XM_024448514.1:c.893+16_893+18del	XP_024304282.1:n.893+16_893+18del
XM_024448515.1:c.893+16_893+18del	XP_024304283.1:n.893+16_893+18del
NM_000019.4:c.1163+16_1163+18del MANE Select	NP_000010.1:n.1163+16_1163+18del
NM_001386677.1:c.1163+16_1163+18del	NP_001373606.1:n.1163+16_1163+18del
NM_001386678.1:c.848+16_848+18del	NP_001373607.1:n.848+16_848+18del
NM_001386679.1:c.866+16_866+18del	NP_001373608.1:n.866+16_866+18del
NM_001386681.1:c.893+16_893+18del	NP_001373610.1:n.893+16_893+18del
NM_001386682.1:c.893+16_893+18del	NP_001373611.1:n.893+16_893+18del
NM_001386685.1:c.893+16_893+18del	NP_001373614.1:n.893+16_893+18del
NM_001386686.1:c.893+16_893+18del	NP_001373615.1:n.893+16_893+18del
NM_001386687.1:c.893+16_893+18del	NP_001373616.1:n.893+16_893+18del
NM_001386688.1:c.893+16_893+18del	NP_001373617.1:n.893+16_893+18del
NM_001386689.1:c.893+16_893+18del	NP_001373618.1:n.893+16_893+18del
NM_001386690.1:c.893+16_893+18del	NP_001373619.1:n.893+16_893+18del
NM_001386691.1:c.893+16_893+18del	NP_001373620.1:n.893+16_893+18del
NR_170162.1:n.1138+16_1138+18del
NR_170163.1:n.1196+16_1196+18del