Canonical Allele Identifier: CA2067543622

Gene: ACADS

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.120727026C= , CM000674.2:g.120727026C=	GRCh38
NC_000012.11:g.121164829C= , CM000674.1:g.121164829C=	GRCh37
NC_000012.10:g.119649212C=	NCBI36
NG_007991.1:g.6259C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242592.9:c.47C= MANE Select	ENSP00000242592.4:p.Ala16=
ENST00000242592.8:c.47C=	ENSP00000242592.4:p.Ala16=
ENST00000411593.2:c.47C=	ENSP00000401045.2:p.Ala16=
ENST00000539690.1:n.159C=
NM_000017.3:c.47C=	NP_000008.1:p.Ala16=
NM_001302554.1:c.47C=	NP_001289483.1:p.Ala16=
NM_000017.4:c.47C= MANE Select	NP_000008.1:p.Ala16=
NM_001302554.2:c.47C=	NP_001289483.1:p.Ala16=