Canonical Allele Identifier: CA386601699

Gene: ACADS

Linked Data

• dbSNP Id: rs768733898
• MyVariant Identifiers: chr12:g.121176979G>T (hg19) ; chr12:g.120739176G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.120739176G>T , CM000674.2:g.120739176G>T	GRCh38
NC_000012.11:g.121176979G>T , CM000674.1:g.121176979G>T	GRCh37
NC_000012.10:g.119661362G>T	NCBI36
NG_007991.1:g.18409G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000242592.9:c.1066G>T MANE Select	ENSP00000242592.4:p.Ala356Ser
ENST00000242592.8:c.1066G>T	ENSP00000242592.4:p.Ala356Ser
ENST00000411593.2:c.1054G>T	ENSP00000401045.2:p.Ala352Ser
NM_000017.3:c.1066G>T	NP_000008.1:p.Ala356Ser
NM_001302554.1:c.1054G>T	NP_001289483.1:p.Ala352Ser
NM_000017.4:c.1066G>T MANE Select	NP_000008.1:p.Ala356Ser
NM_001302554.2:c.1054G>T	NP_001289483.1:p.Ala352Ser