Canonical Allele Identifier: CA2615843003
Gene: ACAT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108143936_108143937insCA , CM000673.2:g.108143936_108143937insCA GRCh38
NC_000011.9:g.108014663_108014664insCA , CM000673.1:g.108014663_108014664insCA GRCh37
NC_000011.8:g.107519873_107519874insCA NCBI36
NG_009888.1:g.27406_27407insCA
NG_009888.2:g.32232_32233insCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000265838.9:c.941-47_941-46insCA MANE Select ENSP00000265838.4:n.941-47_941-46insCA
ENST00000671707.1:n.1036-47_1036-46insCA
ENST00000672031.1:c.940+1386_940+1387insCA ENSP00000500463.1:n.940+1386_940+1387insCA
ENST00000672284.1:c.671-47_671-46insCA ENSP00000500444.1:n.671-47_671-46insCA
ENST00000672354.1:c.941-47_941-46insCA ENSP00000500490.1:n.941-47_941-46insCA
ENST00000672367.1:c.578-47_578-46insCA ENSP00000500209.1:n.578-47_578-46insCA
ENST00000672580.1:c.*196-47_*196-46insCA ENSP00000500366.1:n.*196-47_*196-46insCA
ENST00000672907.1:c.626-47_626-46insCA ENSP00000500928.1:n.626-47_626-46insCA
ENST00000673000.1:n.1029-47_1029-46insCA
ENST00000673531.1:c.671-47_671-46insCA ENSP00000500163.1:n.671-47_671-46insCA
ENST00000265838.8:c.941-47_941-46insCA ENSP00000265838.4:n.941-47_941-46insCA
ENST00000531813.5:c.*1799_*1800insCA ENSP00000435965.1:n.*1799_*1800insCA
ENST00000532792.5:n.436-47_436-46insCA
ENST00000533610.1:n.402-47_402-46insCA
NM_000019.3:c.941-47_941-46insCA NP_000010.1:n.941-47_941-46insCA
XM_006718834.2:c.671-47_671-46insCA XP_006718897.1:n.671-47_671-46insCA
XM_006718835.2:c.671-47_671-46insCA XP_006718898.1:n.671-47_671-46insCA
XM_006718835.3:c.671-47_671-46insCA XP_006718898.1:n.671-47_671-46insCA
XM_017017681.1:c.671-47_671-46insCA XP_016873170.1:n.671-47_671-46insCA
XM_017017682.2:c.563-47_563-46insCA XP_016873171.1:n.563-47_563-46insCA
XM_017017683.2:c.563-47_563-46insCA XP_016873172.1:n.563-47_563-46insCA
XM_024448511.1:c.671-47_671-46insCA XP_024304279.1:n.671-47_671-46insCA
XM_024448512.1:c.671-47_671-46insCA XP_024304280.1:n.671-47_671-46insCA
XM_024448513.1:c.671-47_671-46insCA XP_024304281.1:n.671-47_671-46insCA
XM_024448514.1:c.671-47_671-46insCA XP_024304282.1:n.671-47_671-46insCA
XM_024448515.1:c.671-47_671-46insCA XP_024304283.1:n.671-47_671-46insCA
NM_000019.4:c.941-47_941-46insCA MANE Select NP_000010.1:n.941-47_941-46insCA
NM_001386677.1:c.941-47_941-46insCA NP_001373606.1:n.941-47_941-46insCA
NM_001386678.1:c.626-47_626-46insCA NP_001373607.1:n.626-47_626-46insCA
NM_001386679.1:c.644-47_644-46insCA NP_001373608.1:n.644-47_644-46insCA
NM_001386681.1:c.671-47_671-46insCA NP_001373610.1:n.671-47_671-46insCA
NM_001386682.1:c.671-47_671-46insCA NP_001373611.1:n.671-47_671-46insCA
NM_001386685.1:c.671-47_671-46insCA NP_001373614.1:n.671-47_671-46insCA
NM_001386686.1:c.671-47_671-46insCA NP_001373615.1:n.671-47_671-46insCA
NM_001386687.1:c.671-47_671-46insCA NP_001373616.1:n.671-47_671-46insCA
NM_001386688.1:c.671-47_671-46insCA NP_001373617.1:n.671-47_671-46insCA
NM_001386689.1:c.671-47_671-46insCA NP_001373618.1:n.671-47_671-46insCA
NM_001386690.1:c.671-47_671-46insCA NP_001373619.1:n.671-47_671-46insCA
NM_001386691.1:c.671-47_671-46insCA NP_001373620.1:n.671-47_671-46insCA
NR_170162.1:n.980+1386_980+1387insCA
NR_170163.1:n.974-47_974-46insCA