Canonical Allele Identifier: CA383518920

Gene: ACAD8

Linked Data

• MyVariant Identifiers: chr11:g.134132415T>G (hg19) ; chr11:g.134262521T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134262521T>G , CM000673.2:g.134262521T>G	GRCh38
NC_000011.9:g.134132415T>G , CM000673.1:g.134132415T>G	GRCh37
NC_000011.8:g.133637625T>G	NCBI36
NG_015842.1:g.13982T>G , LRG_448:g.13982T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281182.9:c.1094T>G MANE Select	ENSP00000281182.5:p.Ile365Ser
ENST00000281182.8:c.1094T>G	ENSP00000281182.4:p.Ile365Ser
ENST00000374752.6:c.713T>G	ENSP00000363884.4:p.Ile238Ser
ENST00000524426.5:c.*824T>G	ENSP00000431310.1:n.*824T>G
ENST00000524502.2:n.94T>G
ENST00000524547.5:n.697T>G
ENST00000526026.5:c.*783T>G	ENSP00000431532.1:n.*783T>G
ENST00000531338.5:n.1338T>G
ENST00000533387.5:n.2153T>G
NM_014384.2:c.1094T>G , LRG_448t1:c.1094T>G	NP_055199.1:p.Ile365Ser
XM_005271501.2:c.1094T>G	XP_005271558.1:p.Ile365Ser
XM_011542750.1:c.1094T>G	XP_011541052.1:p.Ile365Ser
XR_947819.1:n.1158T>G
XR_947820.1:n.1546T>G
XR_947821.1:n.1303T>G
XR_947822.1:n.988T>G
XR_947823.1:n.1144T>G
XM_005271505.4:c.*1359T>G	XP_005271562.1:n.*1359T>G
XM_011542750.3:c.1094T>G	XP_011541052.1:p.Ile365Ser
XM_017017542.2:c.1094T>G	XP_016873031.1:p.Ile365Ser
XM_017017543.2:c.1094T>G	XP_016873032.1:p.Ile365Ser
XM_017017544.2:c.*63T>G	XP_016873033.1:n.*63T>G
XM_017017545.2:c.*306T>G	XP_016873034.1:n.*306T>G
XM_017017546.2:c.800T>G	XP_016873035.1:p.Ile267Ser
XM_017017547.2:c.800T>G	XP_016873036.1:p.Ile267Ser
XM_017017548.2:c.*1730T>G	XP_016873037.1:n.*1730T>G
XM_017017549.2:c.*1504T>G	XP_016873038.1:n.*1504T>G
XM_024448437.1:c.*241T>G	XP_024304205.1:n.*241T>G
XM_024448438.1:c.713T>G	XP_024304206.1:p.Ile238Ser
NM_014384.3:c.1094T>G MANE Select	NP_055199.1:p.Ile365Ser