Canonical Allele Identifier: CA2615844761
Gene: ACAT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108147175_108147176insGGTT , CM000673.2:g.108147175_108147176insGGTT GRCh38
NC_000011.9:g.108017902_108017903insGGTT , CM000673.1:g.108017902_108017903insGGTT GRCh37
NC_000011.8:g.107523112_107523113insGGTT NCBI36
NG_009888.1:g.30645_30646insGGTT
NG_009888.2:g.35471_35472insGGTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000265838.9:c.1164-95_1164-94insGGTT MANE Select ENSP00000265838.4:n.1164-95_1164-94insGGTT
ENST00000671707.1:n.1259-95_1259-94insGGTT
ENST00000672031.1:c.*151-95_*151-94insGGTT ENSP00000500463.1:n.*151-95_*151-94insGGTT
ENST00000672284.1:c.894-95_894-94insGGTT ENSP00000500444.1:n.894-95_894-94insGGTT
ENST00000672354.1:c.1164-74_1164-73insGGTT ENSP00000500490.1:n.1164-74_1164-73insGGTT
ENST00000672367.1:c.801-95_801-94insGGTT ENSP00000500209.1:n.801-95_801-94insGGTT
ENST00000672580.1:c.*419-95_*419-94insGGTT ENSP00000500366.1:n.*419-95_*419-94insGGTT
ENST00000672907.1:c.849-95_849-94insGGTT ENSP00000500928.1:n.849-95_849-94insGGTT
ENST00000673000.1:n.1252-95_1252-94insGGTT
ENST00000673531.1:c.894-95_894-94insGGTT ENSP00000500163.1:n.894-95_894-94insGGTT
ENST00000265838.8:c.1164-95_1164-94insGGTT ENSP00000265838.4:n.1164-95_1164-94insGGTT
ENST00000533597.1:n.240-95_240-94insGGTT
NM_000019.3:c.1164-95_1164-94insGGTT NP_000010.1:n.1164-95_1164-94insGGTT
XM_006718834.2:c.894-95_894-94insGGTT XP_006718897.1:n.894-95_894-94insGGTT
XM_006718835.2:c.894-95_894-94insGGTT XP_006718898.1:n.894-95_894-94insGGTT
XM_006718835.3:c.894-95_894-94insGGTT XP_006718898.1:n.894-95_894-94insGGTT
XM_017017681.1:c.894-95_894-94insGGTT XP_016873170.1:n.894-95_894-94insGGTT
XM_017017682.2:c.786-95_786-94insGGTT XP_016873171.1:n.786-95_786-94insGGTT
XM_017017683.2:c.786-95_786-94insGGTT XP_016873172.1:n.786-95_786-94insGGTT
XM_024448511.1:c.894-95_894-94insGGTT XP_024304279.1:n.894-95_894-94insGGTT
XM_024448512.1:c.894-95_894-94insGGTT XP_024304280.1:n.894-95_894-94insGGTT
XM_024448513.1:c.894-95_894-94insGGTT XP_024304281.1:n.894-95_894-94insGGTT
XM_024448514.1:c.894-95_894-94insGGTT XP_024304282.1:n.894-95_894-94insGGTT
XM_024448515.1:c.894-95_894-94insGGTT XP_024304283.1:n.894-95_894-94insGGTT
NM_000019.4:c.1164-95_1164-94insGGTT MANE Select NP_000010.1:n.1164-95_1164-94insGGTT
NM_001386677.1:c.1164-74_1164-73insGGTT NP_001373606.1:n.1164-74_1164-73insGGTT
NM_001386678.1:c.849-95_849-94insGGTT NP_001373607.1:n.849-95_849-94insGGTT
NM_001386679.1:c.867-95_867-94insGGTT NP_001373608.1:n.867-95_867-94insGGTT
NM_001386681.1:c.894-95_894-94insGGTT NP_001373610.1:n.894-95_894-94insGGTT
NM_001386682.1:c.894-95_894-94insGGTT NP_001373611.1:n.894-95_894-94insGGTT
NM_001386685.1:c.894-95_894-94insGGTT NP_001373614.1:n.894-95_894-94insGGTT
NM_001386686.1:c.894-95_894-94insGGTT NP_001373615.1:n.894-95_894-94insGGTT
NM_001386687.1:c.894-95_894-94insGGTT NP_001373616.1:n.894-95_894-94insGGTT
NM_001386688.1:c.894-95_894-94insGGTT NP_001373617.1:n.894-95_894-94insGGTT
NM_001386689.1:c.894-95_894-94insGGTT NP_001373618.1:n.894-95_894-94insGGTT
NM_001386690.1:c.894-95_894-94insGGTT NP_001373619.1:n.894-95_894-94insGGTT
NM_001386691.1:c.894-95_894-94insGGTT NP_001373620.1:n.894-95_894-94insGGTT
NR_170162.1:n.1139-95_1139-94insGGTT
NR_170163.1:n.1197-95_1197-94insGGTT