Canonical Allele Identifier: CA655233547

Gene: ACADS

Linked Data

• COSMIC: COSN26552259

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.120739229G>T , CM000674.2:g.120739229G>T	GRCh38
NC_000012.11:g.121177032G>T , CM000674.1:g.121177032G>T	GRCh37
NC_000012.10:g.119661415G>T	NCBI36
NG_007991.1:g.18462G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000242592.9:c.1086+33G>T MANE Select	ENSP00000242592.4:n.1086+33G>T
ENST00000242592.8:c.1086+33G>T	ENSP00000242592.4:n.1086+33G>T
ENST00000411593.2:c.1074+33G>T	ENSP00000401045.2:n.1074+33G>T
NM_000017.3:c.1086+33G>T	NP_000008.1:n.1086+33G>T
NM_001302554.1:c.1074+33G>T	NP_001289483.1:n.1074+33G>T
NM_000017.4:c.1086+33G>T MANE Select	NP_000008.1:n.1086+33G>T
NM_001302554.2:c.1074+33G>T	NP_001289483.1:n.1074+33G>T