Canonical Allele Identifier: CA602656831

Gene: ACAD8

Linked Data

• gnomAD v2: 11-134132348-G-C
• MyVariant Identifiers: chr11:g.134132348G>C (hg19) ; chr11:g.134262454G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134262454G>C , CM000673.2:g.134262454G>C	GRCh38
NC_000011.9:g.134132348G>C , CM000673.1:g.134132348G>C	GRCh37
NC_000011.8:g.133637558G>C	NCBI36
NG_015842.1:g.13915G>C , LRG_448:g.13915G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281182.9:c.1093-66G>C MANE Select	ENSP00000281182.5:n.1093-66G>C
ENST00000281182.8:c.1093-66G>C	ENSP00000281182.4:n.1093-66G>C
ENST00000374752.6:c.712-66G>C	ENSP00000363884.4:n.712-66G>C
ENST00000524426.5:c.*823-66G>C	ENSP00000431310.1:n.*823-66G>C
ENST00000524502.2:n.93-66G>C
ENST00000524547.5:n.696-66G>C
ENST00000526026.5:c.*782-66G>C	ENSP00000431532.1:n.*782-66G>C
ENST00000531338.5:n.1271G>C
ENST00000533387.5:n.2152-66G>C
NM_014384.2:c.1093-66G>C , LRG_448t1:c.1093-66G>C	NP_055199.1:n.1093-66G>C
XM_005271501.2:c.1093-66G>C	XP_005271558.1:n.1093-66G>C
XM_011542750.1:c.1093-66G>C	XP_011541052.1:n.1093-66G>C
XR_947819.1:n.1157-66G>C
XR_947820.1:n.1479G>C
XR_947821.1:n.1302-66G>C
XR_947822.1:n.987-66G>C
XR_947823.1:n.1143-66G>C
XM_005271505.4:c.*1358-66G>C	XP_005271562.1:n.*1358-66G>C
XM_011542750.3:c.1093-66G>C	XP_011541052.1:n.1093-66G>C
XM_017017542.2:c.1093-66G>C	XP_016873031.1:n.1093-66G>C
XM_017017543.2:c.1093-66G>C	XP_016873032.1:n.1093-66G>C
XM_017017544.2:c.*62-66G>C	XP_016873033.1:n.*62-66G>C
XM_017017545.2:c.*239G>C	XP_016873034.1:n.*239G>C
XM_017017546.2:c.799-66G>C	XP_016873035.1:n.799-66G>C
XM_017017547.2:c.799-66G>C	XP_016873036.1:n.799-66G>C
XM_017017548.2:c.*1729-66G>C	XP_016873037.1:n.*1729-66G>C
XM_017017549.2:c.*1503-66G>C	XP_016873038.1:n.*1503-66G>C
XM_024448437.1:c.*174G>C	XP_024304205.1:n.*174G>C
XM_024448438.1:c.712-66G>C	XP_024304206.1:n.712-66G>C
NM_014384.3:c.1093-66G>C MANE Select	NP_055199.1:n.1093-66G>C