Canonical Allele Identifier: CA7260330
Gene: ACOT1 HGNC NCBI
HEATR4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.73537571G>A , CM000676.2:g.73537571G>A GRCh38
NC_000014.8:g.74004275G>A , CM000676.1:g.74004275G>A GRCh37
NC_000014.7:g.73074028G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001037161.2:c.150G>A (ACOT1) MANE Select NP_001032238.1:p.Ala50=
NM_001220484.1:c.-151-7327C>T (HEATR4) MANE Select NP_001207413.1:n.-151-7327C>T
ENST00000311148.9:c.150G>A (ACOT1) MANE Select ENSP00000311224.4:p.Ala50=
ENST00000553558.6:c.-151-7327C>T (HEATR4) MANE Select ENSP00000450444.2:n.-151-7327C>T
NM_001037161.1:c.150G>A (ACOT1) NP_001032238.1:p.Ala50=
NM_203309.2:c.-72-14347C>T (HEATR4) NP_976054.2:n.-72-14347C>T
ENST00000311148.8:c.150G>A (ACOT1) ENSP00000311224.4:p.Ala50=
ENST00000334988.2:c.-72-14347C>T (HEATR4) ENSP00000335447.2:n.-72-14347C>T
ENST00000553558.5:c.-151-7327C>T (HEATR4) ENSP00000450444.1:n.-151-7327C>T
ENST00000557556.1:c.150G>A (ACOT1) ENSP00000451764.1:p.Ala50=
ENST00000563329.1:c.-320-7327C>T (HEATR4) ENSP00000456792.1:n.-320-7327C>T
XM_011537075.1:c.89-3922G>A (ACOT1) XP_011535377.1:n.89-3922G>A
XM_017021590.1:c.89-3922G>A (ACOT1) XP_016877079.1:n.89-3922G>A
XM_017021591.1:c.-29-3922G>A (ACOT1) XP_016877080.1:n.-29-3922G>A
XM_017021592.1:c.-29-3922G>A (ACOT1) XP_016877081.1:n.-29-3922G>A