Canonical Allele Identifier: CA2616919038

Gene: ACAD8

Linked Data

• gnomAD v4: 11-134262860-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134262860G>C , CM000673.2:g.134262860G>C	GRCh38
NC_000011.9:g.134132754G>C , CM000673.1:g.134132754G>C	GRCh37
NC_000011.8:g.133637964G>C	NCBI36
NG_015842.1:g.14321G>C , LRG_448:g.14321G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281182.9:c.1195+238G>C MANE Select	ENSP00000281182.5:n.1195+238G>C
ENST00000281182.8:c.1195+238G>C	ENSP00000281182.4:n.1195+238G>C
ENST00000374752.6:c.814+238G>C	ENSP00000363884.4:n.814+238G>C
ENST00000524502.2:n.286G>C
ENST00000526026.5:c.*975G>C	ENSP00000431532.1:n.*975G>C
ENST00000531338.5:n.1677G>C
ENST00000533387.5:n.2254+238G>C
NM_014384.2:c.1195+238G>C , LRG_448t1:c.1195+238G>C	NP_055199.1:n.1195+238G>C
XM_005271501.2:c.1286G>C	XP_005271558.1:p.Gly429Ala
XM_011542750.1:c.1195+238G>C	XP_011541052.1:n.1195+238G>C
XR_947819.1:n.1259+238G>C
XR_947820.1:n.1885G>C
XR_947822.1:n.1089+238G>C
XR_947823.1:n.1245+238G>C
XM_005271505.4:c.*1460+238G>C	XP_005271562.1:n.*1460+238G>C
XM_011542750.3:c.1195+238G>C	XP_011541052.1:n.1195+238G>C
XM_017017542.2:c.1195+238G>C	XP_016873031.1:n.1195+238G>C
XM_017017543.2:c.1286G>C	XP_016873032.1:p.Gly429Ala
XM_017017544.2:c.*164+238G>C	XP_016873033.1:n.*164+238G>C
XM_017017545.2:c.*645G>C	XP_016873034.1:n.*645G>C
XM_017017546.2:c.901+238G>C	XP_016873035.1:n.901+238G>C
XM_017017547.2:c.901+238G>C	XP_016873036.1:n.901+238G>C
XM_017017548.2:c.*1922G>C	XP_016873037.1:n.*1922G>C
XM_017017549.2:c.*1605+238G>C	XP_016873038.1:n.*1605+238G>C
XM_024448437.1:c.*580G>C	XP_024304205.1:n.*580G>C
XM_024448438.1:c.814+238G>C	XP_024304206.1:n.814+238G>C
NM_014384.3:c.1195+238G>C MANE Select	NP_055199.1:n.1195+238G>C