Canonical Allele Identifier: CA383519282

Gene: ACAD8

Linked Data

• MyVariant Identifiers: chr11:g.134132481A>C (hg19) ; chr11:g.134262587A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134262587A>C , CM000673.2:g.134262587A>C	GRCh38
NC_000011.9:g.134132481A>C , CM000673.1:g.134132481A>C	GRCh37
NC_000011.8:g.133637691A>C	NCBI36
NG_015842.1:g.14048A>C , LRG_448:g.14048A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281182.9:c.1160A>C MANE Select	ENSP00000281182.5:p.Tyr387Ser
ENST00000281182.8:c.1160A>C	ENSP00000281182.4:p.Tyr387Ser
ENST00000374752.6:c.779A>C	ENSP00000363884.4:p.Tyr260Ser
ENST00000524426.5:c.*890A>C	ENSP00000431310.1:n.*890A>C
ENST00000524502.2:n.160A>C
ENST00000526026.5:c.*849A>C	ENSP00000431532.1:n.*849A>C
ENST00000531338.5:n.1404A>C
ENST00000533387.5:n.2219A>C
NM_014384.2:c.1160A>C , LRG_448t1:c.1160A>C	NP_055199.1:p.Tyr387Ser
XM_005271501.2:c.1160A>C	XP_005271558.1:p.Tyr387Ser
XM_011542750.1:c.1160A>C	XP_011541052.1:p.Tyr387Ser
XR_947819.1:n.1224A>C
XR_947820.1:n.1612A>C
XR_947821.1:n.1369A>C
XR_947822.1:n.1054A>C
XR_947823.1:n.1210A>C
XM_005271505.4:c.*1425A>C	XP_005271562.1:n.*1425A>C
XM_011542750.3:c.1160A>C	XP_011541052.1:p.Tyr387Ser
XM_017017542.2:c.1160A>C	XP_016873031.1:p.Tyr387Ser
XM_017017543.2:c.1160A>C	XP_016873032.1:p.Tyr387Ser
XM_017017544.2:c.*129A>C	XP_016873033.1:n.*129A>C
XM_017017545.2:c.*372A>C	XP_016873034.1:n.*372A>C
XM_017017546.2:c.866A>C	XP_016873035.1:p.Tyr289Ser
XM_017017547.2:c.866A>C	XP_016873036.1:p.Tyr289Ser
XM_017017548.2:c.*1796A>C	XP_016873037.1:n.*1796A>C
XM_017017549.2:c.*1570A>C	XP_016873038.1:n.*1570A>C
XM_024448437.1:c.*307A>C	XP_024304205.1:n.*307A>C
XM_024448438.1:c.779A>C	XP_024304206.1:p.Tyr260Ser
NM_014384.3:c.1160A>C MANE Select	NP_055199.1:p.Tyr387Ser