Canonical Allele Identifier: CA383518950

Gene: ACAD8

Linked Data

• MyVariant Identifiers: chr11:g.134132420A>C (hg19) ; chr11:g.134262526A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134262526A>C , CM000673.2:g.134262526A>C	GRCh38
NC_000011.9:g.134132420A>C , CM000673.1:g.134132420A>C	GRCh37
NC_000011.8:g.133637630A>C	NCBI36
NG_015842.1:g.13987A>C , LRG_448:g.13987A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281182.9:c.1099A>C MANE Select	ENSP00000281182.5:p.Asn367His
ENST00000281182.8:c.1099A>C	ENSP00000281182.4:p.Asn367His
ENST00000374752.6:c.718A>C	ENSP00000363884.4:p.Asn240His
ENST00000524426.5:c.*829A>C	ENSP00000431310.1:n.*829A>C
ENST00000524502.2:n.99A>C
ENST00000524547.5:n.702A>C
ENST00000526026.5:c.*788A>C	ENSP00000431532.1:n.*788A>C
ENST00000531338.5:n.1343A>C
ENST00000533387.5:n.2158A>C
NM_014384.2:c.1099A>C , LRG_448t1:c.1099A>C	NP_055199.1:p.Asn367His
XM_005271501.2:c.1099A>C	XP_005271558.1:p.Asn367His
XM_011542750.1:c.1099A>C	XP_011541052.1:p.Asn367His
XR_947819.1:n.1163A>C
XR_947820.1:n.1551A>C
XR_947821.1:n.1308A>C
XR_947822.1:n.993A>C
XR_947823.1:n.1149A>C
XM_005271505.4:c.*1364A>C	XP_005271562.1:n.*1364A>C
XM_011542750.3:c.1099A>C	XP_011541052.1:p.Asn367His
XM_017017542.2:c.1099A>C	XP_016873031.1:p.Asn367His
XM_017017543.2:c.1099A>C	XP_016873032.1:p.Asn367His
XM_017017544.2:c.*68A>C	XP_016873033.1:n.*68A>C
XM_017017545.2:c.*311A>C	XP_016873034.1:n.*311A>C
XM_017017546.2:c.805A>C	XP_016873035.1:p.Asn269His
XM_017017547.2:c.805A>C	XP_016873036.1:p.Asn269His
XM_017017548.2:c.*1735A>C	XP_016873037.1:n.*1735A>C
XM_017017549.2:c.*1509A>C	XP_016873038.1:n.*1509A>C
XM_024448437.1:c.*246A>C	XP_024304205.1:n.*246A>C
XM_024448438.1:c.718A>C	XP_024304206.1:p.Asn240His
NM_014384.3:c.1099A>C MANE Select	NP_055199.1:p.Asn367His