Canonical Allele Identifier: CA2621371493

Gene: ACADS

Linked Data

• gnomAD v4: 12-120739709-G-GT

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.120739709_120739710insT , CM000674.2:g.120739709_120739710insT	GRCh38
NC_000012.11:g.121177512_121177513insT , CM000674.1:g.121177512_121177513insT	GRCh37
NC_000012.10:g.119661895_119661896insT	NCBI36
NG_007991.1:g.18942_18943insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242592.9:c.*261_*262insT MANE Select	ENSP00000242592.4:n.*261_*262insT
ENST00000242592.8:c.*261_*262insT	ENSP00000242592.4:n.*261_*262insT
NM_000017.3:c.*261_*262insT	NP_000008.1:n.*261_*262insT
NM_001302554.1:c.*261_*262insT	NP_001289483.1:n.*261_*262insT
NM_000017.4:c.*261_*262insT MANE Select	NP_000008.1:n.*261_*262insT
NM_001302554.2:c.*261_*262insT	NP_001289483.1:n.*261_*262insT