Canonical Allele Identifier: CA397723007

Gene: ACADVL

Linked Data

• MyVariant Identifiers: chr17:g.7124863C>G (hg19) ; chr17:g.7221544C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7221544C>G , CM000679.2:g.7221544C>G	GRCh38
NC_000017.10:g.7124863C>G , CM000679.1:g.7124863C>G	GRCh37
NC_000017.9:g.7065587C>G	NCBI36
NG_007975.1:g.6711C>G
NG_008391.2:g.3507G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000356839.10:c.484C>G MANE Select	ENSP00000349297.5:p.Arg162Gly
ENST00000322910.9:c.*439C>G	ENSP00000325395.5:n.*439C>G
ENST00000350303.9:c.418C>G	ENSP00000344152.5:p.Arg140Gly
ENST00000356839.9:c.484C>G	ENSP00000349297.5:p.Arg162Gly
ENST00000543245.6:c.553C>G	ENSP00000438689.2:p.Arg185Gly
ENST00000577191.5:n.561C>G
ENST00000577433.5:n.692C>G
ENST00000577857.5:n.300C>G
ENST00000579286.5:n.665C>G
ENST00000579886.2:c.322C>G	ENSP00000463246.1:p.Arg108Gly
ENST00000580365.1:n.215C>G
ENST00000581378.5:c.202C>G
ENST00000581562.5:n.525-408C>G
ENST00000582166.1:n.465C>G
ENST00000583312.5:c.484C>G	ENSP00000467920.1:p.Arg162Gly
ENST00000583760.1:n.266C>G
NM_000018.3:c.484C>G	NP_000009.1:p.Arg162Gly
NM_001033859.2:c.418C>G	NP_001029031.1:p.Arg140Gly
NM_001270447.1:c.553C>G	NP_001257376.1:p.Arg185Gly
NM_001270448.1:c.256C>G	NP_001257377.1:p.Arg86Gly
XM_006721516.2:c.484C>G	XP_006721579.2:p.Arg162Gly
XM_011523829.1:c.484C>G	XP_011522131.1:p.Arg162Gly
XM_011523830.1:c.484C>G	XP_011522132.1:p.Arg162Gly
XR_934021.1:n.591C>G
XR_934022.1:n.591C>G
XR_934023.1:n.591C>G
XM_006721516.3:c.484C>G	XP_006721579.2:p.Arg162Gly
XM_011523829.2:c.484C>G	XP_011522131.1:p.Arg162Gly
XM_011523830.2:c.484C>G	XP_011522132.1:p.Arg162Gly
XM_024450741.1:c.484C>G	XP_024306509.1:p.Arg162Gly
XR_934021.2:n.543C>G
XR_934022.2:n.543C>G
XR_934023.2:n.543C>G
NM_000018.4:c.484C>G MANE Select	NP_000009.1:p.Arg162Gly
NM_001033859.3:c.418C>G	NP_001029031.1:p.Arg140Gly
NM_001270447.2:c.553C>G	NP_001257376.1:p.Arg185Gly
NM_001270448.2:c.256C>G	NP_001257377.1:p.Arg86Gly