Canonical Allele Identifier: CA2616919089

Gene: ACAD8

Linked Data

• dbSNP Id: rs2136084943
• gnomAD v4: 11-134262916-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134262916C>T , CM000673.2:g.134262916C>T	GRCh38
NC_000011.9:g.134132810C>T , CM000673.1:g.134132810C>T	GRCh37
NC_000011.8:g.133638020C>T	NCBI36
NG_015842.1:g.14377C>T , LRG_448:g.14377C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281182.9:c.1195+294C>T MANE Select	ENSP00000281182.5:n.1195+294C>T
ENST00000281182.8:c.1195+294C>T	ENSP00000281182.4:n.1195+294C>T
ENST00000374752.6:c.814+294C>T	ENSP00000363884.4:n.814+294C>T
ENST00000524502.2:n.342C>T
ENST00000526026.5:c.*1031C>T	ENSP00000431532.1:n.*1031C>T
ENST00000531338.5:n.1733C>T
ENST00000533387.5:n.2254+294C>T
NM_014384.2:c.1195+294C>T , LRG_448t1:c.1195+294C>T	NP_055199.1:n.1195+294C>T
XM_005271501.2:c.*37C>T	XP_005271558.1:n.*37C>T
XM_011542750.1:c.1195+294C>T	XP_011541052.1:n.1195+294C>T
XR_947819.1:n.1259+294C>T
XR_947820.1:n.1941C>T
XR_947822.1:n.1089+294C>T
XR_947823.1:n.1245+294C>T
XM_005271505.4:c.*1460+294C>T	XP_005271562.1:n.*1460+294C>T
XM_011542750.3:c.1195+294C>T	XP_011541052.1:n.1195+294C>T
XM_017017542.2:c.1195+294C>T	XP_016873031.1:n.1195+294C>T
XM_017017543.2:c.*37C>T	XP_016873032.1:n.*37C>T
XM_017017544.2:c.*164+294C>T	XP_016873033.1:n.*164+294C>T
XM_017017545.2:c.*701C>T	XP_016873034.1:n.*701C>T
XM_017017546.2:c.901+294C>T	XP_016873035.1:n.901+294C>T
XM_017017547.2:c.901+294C>T	XP_016873036.1:n.901+294C>T
XM_017017548.2:c.*1978C>T	XP_016873037.1:n.*1978C>T
XM_017017549.2:c.*1605+294C>T	XP_016873038.1:n.*1605+294C>T
XM_024448437.1:c.*636C>T	XP_024304205.1:n.*636C>T
XM_024448438.1:c.814+294C>T	XP_024304206.1:n.814+294C>T
NM_014384.3:c.1195+294C>T MANE Select	NP_055199.1:n.1195+294C>T