Canonical Allele Identifier: CA383518969

Gene: ACAD8

Linked Data

• MyVariant Identifiers: chr11:g.134132423C>T (hg19) ; chr11:g.134262529C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134262529C>T , CM000673.2:g.134262529C>T	GRCh38
NC_000011.9:g.134132423C>T , CM000673.1:g.134132423C>T	GRCh37
NC_000011.8:g.133637633C>T	NCBI36
NG_015842.1:g.13990C>T , LRG_448:g.13990C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281182.9:c.1102C>T MANE Select	ENSP00000281182.5:p.Gln368Ter
ENST00000281182.8:c.1102C>T	ENSP00000281182.4:p.Gln368Ter
ENST00000374752.6:c.721C>T	ENSP00000363884.4:p.Gln241Ter
ENST00000524426.5:c.*832C>T	ENSP00000431310.1:n.*832C>T
ENST00000524502.2:n.102C>T
ENST00000526026.5:c.*791C>T	ENSP00000431532.1:n.*791C>T
ENST00000531338.5:n.1346C>T
ENST00000533387.5:n.2161C>T
NM_014384.2:c.1102C>T , LRG_448t1:c.1102C>T	NP_055199.1:p.Gln368Ter
XM_005271501.2:c.1102C>T	XP_005271558.1:p.Gln368Ter
XM_011542750.1:c.1102C>T	XP_011541052.1:p.Gln368Ter
XR_947819.1:n.1166C>T
XR_947820.1:n.1554C>T
XR_947821.1:n.1311C>T
XR_947822.1:n.996C>T
XR_947823.1:n.1152C>T
XM_005271505.4:c.*1367C>T	XP_005271562.1:n.*1367C>T
XM_011542750.3:c.1102C>T	XP_011541052.1:p.Gln368Ter
XM_017017542.2:c.1102C>T	XP_016873031.1:p.Gln368Ter
XM_017017543.2:c.1102C>T	XP_016873032.1:p.Gln368Ter
XM_017017544.2:c.*71C>T	XP_016873033.1:n.*71C>T
XM_017017545.2:c.*314C>T	XP_016873034.1:n.*314C>T
XM_017017546.2:c.808C>T	XP_016873035.1:p.Gln270Ter
XM_017017547.2:c.808C>T	XP_016873036.1:p.Gln270Ter
XM_017017548.2:c.*1738C>T	XP_016873037.1:n.*1738C>T
XM_017017549.2:c.*1512C>T	XP_016873038.1:n.*1512C>T
XM_024448437.1:c.*249C>T	XP_024304205.1:n.*249C>T
XM_024448438.1:c.721C>T	XP_024304206.1:p.Gln241Ter
NM_014384.3:c.1102C>T MANE Select	NP_055199.1:p.Gln368Ter