Canonical Allele Identifier: CA2574378669

Gene: ACOT11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.54609173_54609177del , CM000663.2:g.54609173_54609177del	GRCh38
NC_000001.10:g.55074846_55074850del , CM000663.1:g.55074846_55074850del	GRCh37
NC_000001.9:g.54847434_54847438del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343744.7:c.*61_*65del MANE Select	ENSP00000340260.2:n.*61_*65del
ENST00000343744.6:c.*61_*65del	ENSP00000340260.2:n.*61_*65del
ENST00000371316.3:c.1629+1105_1629+1109del	ENSP00000360366.3:n.1629+1105_1629+1109del
ENST00000481208.5:n.1924_1928del
NM_015547.3:c.1629+1105_1629+1109del	NP_056362.1:n.1629+1105_1629+1109del
NM_147161.3:c.*61_*65del	NP_671517.1:n.*61_*65del
NM_015547.4:c.1629+1105_1629+1109del	NP_056362.1:n.1629+1105_1629+1109del
NM_147161.4:c.*61_*65del MANE Select	NP_671517.1:n.*61_*65del