Canonical Allele Identifier: CA354438502

Gene: ACAD9

Linked Data

• MyVariant Identifiers: chr3:g.128628196A>T (hg19) ; chr3:g.128909353A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128909353A>T , CM000665.2:g.128909353A>T	GRCh38
NC_000003.11:g.128628196A>T , CM000665.1:g.128628196A>T	GRCh37
NC_000003.10:g.130110886A>T	NCBI36
NG_017064.1:g.34864A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.1495A>T MANE Select	ENSP00000312618.7:p.Asn499Tyr
ENST00000511325.2:n.1573A>T
ENST00000679399.1:c.*1666A>T	ENSP00000505434.1:n.*1666A>T
ENST00000679431.1:c.*1371A>T	ENSP00000506440.1:n.*1371A>T
ENST00000679613.1:c.1495A>T	ENSP00000504971.1:p.Asn499Tyr
ENST00000679715.1:c.1126A>T	ENSP00000506228.1:p.Asn376Tyr
ENST00000679824.1:c.*2801A>T	ENSP00000505516.1:n.*2801A>T
ENST00000679990.1:n.1730A>T
ENST00000680636.1:c.1495A>T	ENSP00000504886.1:p.Asn499Tyr
ENST00000680638.1:n.1248A>T
ENST00000680744.1:c.*848A>T	ENSP00000505243.1:n.*848A>T
ENST00000680764.1:c.*2899A>T	ENSP00000505126.1:n.*2899A>T
ENST00000681319.1:n.2281A>T
ENST00000681367.1:c.1495A>T	ENSP00000505309.1:p.Asn499Tyr
ENST00000681552.1:c.1150-3154A>T	ENSP00000505699.1:n.1150-3154A>T
ENST00000681583.1:c.1495A>T	ENSP00000506340.1:p.Asn499Tyr
ENST00000681585.1:c.*114A>T	ENSP00000506316.1:n.*114A>T
ENST00000681784.1:n.1573A>T
ENST00000681886.1:c.*688A>T	ENSP00000506500.1:n.*688A>T
ENST00000308982.11:c.1495A>T	ENSP00000312618.7:p.Asn499Tyr
ENST00000505867.5:c.*1295A>T	ENSP00000425346.1:n.*1295A>T
ENST00000508971.1:c.784A>T	ENSP00000422683.1:p.Asn262Tyr
ENST00000511227.5:c.*1389A>T	ENSP00000425226.1:n.*1389A>T
ENST00000511325.1:n.476A>T
ENST00000511526.5:n.1028A>T
NM_014049.4:c.1495A>T	NP_054768.2:p.Asn499Tyr
NR_033426.1:n.1873A>T
XM_011512742.1:c.1126A>T	XP_011511044.1:p.Asn376Tyr
XM_024453484.1:c.1126A>T	XP_024309252.1:p.Asn376Tyr
XM_024453485.1:c.1126A>T	XP_024309253.1:p.Asn376Tyr
XR_427367.3:n.1571A>T
NM_014049.5:c.1495A>T MANE Select	NP_054768.2:p.Asn499Tyr
NR_033426.2:n.1743A>T