Canonical Allele Identifier: CA2667560233

Gene: ACAD9

Linked Data

• gnomAD v4: 3-128904013-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128904013G>T , CM000665.2:g.128904013G>T	GRCh38
NC_000003.11:g.128622856G>T , CM000665.1:g.128622856G>T	GRCh37
NC_000003.10:g.130105546G>T	NCBI36
NG_017064.1:g.29524G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.959-49G>T MANE Select	ENSP00000312618.7:n.959-49G>T
ENST00000511325.2:n.1037-49G>T
ENST00000679399.1:c.*853-49G>T	ENSP00000505434.1:n.*853-49G>T
ENST00000679431.1:c.*835-49G>T	ENSP00000506440.1:n.*835-49G>T
ENST00000679613.1:c.959-49G>T	ENSP00000504971.1:n.959-49G>T
ENST00000679715.1:c.590-49G>T	ENSP00000506228.1:n.590-49G>T
ENST00000679824.1:c.*2265-49G>T	ENSP00000505516.1:n.*2265-49G>T
ENST00000679990.1:n.1194-49G>T
ENST00000680636.1:c.959-49G>T	ENSP00000504886.1:n.959-49G>T
ENST00000680744.1:c.*312-49G>T	ENSP00000505243.1:n.*312-49G>T
ENST00000680764.1:c.*2363-49G>T	ENSP00000505126.1:n.*2363-49G>T
ENST00000681319.1:n.1037-49G>T
ENST00000681367.1:c.959-49G>T	ENSP00000505309.1:n.959-49G>T
ENST00000681552.1:c.959-49G>T	ENSP00000505699.1:n.959-49G>T
ENST00000681583.1:c.959-49G>T	ENSP00000506340.1:n.959-49G>T
ENST00000681585.1:c.959-49G>T	ENSP00000506316.1:n.959-49G>T
ENST00000681589.1:n.1173-49G>T
ENST00000681784.1:n.1037-49G>T
ENST00000681886.1:c.*152-49G>T	ENSP00000506500.1:n.*152-49G>T
ENST00000308982.11:c.959-49G>T	ENSP00000312618.7:n.959-49G>T
ENST00000505192.5:c.*655-49G>T	ENSP00000426277.1:n.*655-49G>T
ENST00000505867.5:c.*759-49G>T	ENSP00000425346.1:n.*759-49G>T
ENST00000508971.1:c.248-49G>T	ENSP00000422683.1:n.248-49G>T
ENST00000511227.5:c.*853-49G>T	ENSP00000425226.1:n.*853-49G>T
ENST00000511526.5:n.464-49G>T
NM_014049.4:c.959-49G>T	NP_054768.2:n.959-49G>T
NR_033426.1:n.1337-49G>T
XM_011512742.1:c.590-49G>T	XP_011511044.1:n.590-49G>T
XR_427367.1:n.1035-49G>T
XM_024453484.1:c.590-49G>T	XP_024309252.1:n.590-49G>T
XM_024453485.1:c.590-49G>T	XP_024309253.1:n.590-49G>T
XR_427367.3:n.1035-49G>T
NM_014049.5:c.959-49G>T MANE Select	NP_054768.2:n.959-49G>T
NR_033426.2:n.1207-49G>T