Canonical Allele Identifier: CA397725417

Gene: ACADVL

Linked Data

• MyVariant Identifiers: chr17:g.7127687C>G (hg19) ; chr17:g.7224368C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7224368C>G , CM000679.2:g.7224368C>G	GRCh38
NC_000017.10:g.7127687C>G , CM000679.1:g.7127687C>G	GRCh37
NC_000017.9:g.7068411C>G	NCBI36
NG_007975.1:g.9535C>G
NG_008391.2:g.683G>C
NG_033038.1:g.15177G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.1580C>G MANE Select	ENSP00000349297.5:p.Pro527Arg
ENST00000322910.9:c.*1535C>G	ENSP00000325395.5:n.*1535C>G
ENST00000350303.9:c.1514C>G	ENSP00000344152.5:p.Pro505Arg
ENST00000356839.9:c.1580C>G	ENSP00000349297.5:p.Pro527Arg
ENST00000542255.6:c.438C>G
ENST00000543245.6:c.1649C>G	ENSP00000438689.2:p.Pro550Arg
ENST00000578319.5:n.75C>G
ENST00000578711.1:n.864C>G
ENST00000578809.5:n.152C>G
ENST00000579391.1:n.188C>G
ENST00000579425.5:n.696C>G
ENST00000579546.1:c.319C>G
ENST00000579894.5:n.367C>G
ENST00000582450.1:n.88C>G
ENST00000583074.5:n.201C>G
ENST00000583850.5:n.355C>G
ENST00000583858.5:c.511C>G
ENST00000585203.6:n.771C>G
NM_000018.3:c.1580C>G	NP_000009.1:p.Pro527Arg
NM_001033859.2:c.1514C>G	NP_001029031.1:p.Pro505Arg
NM_001270447.1:c.1649C>G	NP_001257376.1:p.Pro550Arg
NM_001270448.1:c.1352C>G	NP_001257377.1:p.Pro451Arg
XM_006721516.2:c.1580C>G	XP_006721579.2:p.Pro527Arg
XM_011523829.1:c.1482C>G	XP_011522131.1:p.Pro494=
XM_011523830.1:c.1482C>G	XP_011522132.1:p.Pro494=
XR_934021.1:n.1687C>G
XR_934022.1:n.1589C>G
XR_934023.1:n.1589C>G
XM_006721516.3:c.1580C>G	XP_006721579.2:p.Pro527Arg
XM_011523829.2:c.1482C>G	XP_011522131.1:p.Pro494=
XM_011523830.2:c.1482C>G	XP_011522132.1:p.Pro494=
XM_024450741.1:c.1482C>G	XP_024306509.1:p.Pro494=
XR_934021.2:n.1639C>G
XR_934022.2:n.1541C>G
XR_934023.2:n.1541C>G
NM_000018.4:c.1580C>G MANE Select	NP_000009.1:p.Pro527Arg
NM_001033859.3:c.1514C>G	NP_001029031.1:p.Pro505Arg
NM_001270447.2:c.1649C>G	NP_001257376.1:p.Pro550Arg
NM_001270448.2:c.1352C>G	NP_001257377.1:p.Pro451Arg