Canonical Allele Identifier: CA397722097

Gene: ACADVL

Linked Data

• MyVariant Identifiers: chr17:g.7123482C>G (hg19) ; chr17:g.7220163C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7220163C>G , CM000679.2:g.7220163C>G	GRCh38
NC_000017.10:g.7123482C>G , CM000679.1:g.7123482C>G	GRCh37
NC_000017.9:g.7064206C>G	NCBI36
NG_007975.1:g.5330C>G
NG_008391.2:g.4888G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.104C>G MANE Select	ENSP00000349297.5:p.Pro35Arg
ENST00000322910.9:c.*59C>G	ENSP00000325395.5:n.*59C>G
ENST00000350303.9:c.104C>G	ENSP00000344152.5:p.Pro35Arg
ENST00000356839.9:c.104C>G	ENSP00000349297.5:p.Pro35Arg
ENST00000543245.6:c.173C>G	ENSP00000438689.2:p.Pro58Arg
ENST00000577191.5:n.181C>G
ENST00000577857.5:n.194C>G
ENST00000578269.5:n.211C>G
ENST00000578421.1:n.238C>G
ENST00000579286.5:n.211C>G
ENST00000579886.2:c.104C>G	ENSP00000463246.1:p.Pro35Arg
ENST00000580263.5:n.194C>G
ENST00000581562.5:n.151C>G
ENST00000582056.5:n.194C>G
ENST00000582356.5:n.229C>G
ENST00000583312.5:c.104C>G	ENSP00000467920.1:p.Pro35Arg
ENST00000584103.5:c.104C>G	ENSP00000465353.1:p.Pro35Arg
NM_000018.3:c.104C>G	NP_000009.1:p.Pro35Arg
NM_001033859.2:c.104C>G	NP_001029031.1:p.Pro35Arg
NM_001270447.1:c.173C>G	NP_001257376.1:p.Pro58Arg
NM_001270448.1:c.-125C>G	NP_001257377.1:n.-125C>G
XM_006721516.2:c.104C>G	XP_006721579.2:p.Pro35Arg
XM_011523829.1:c.104C>G	XP_011522131.1:p.Pro35Arg
XM_011523830.1:c.104C>G	XP_011522132.1:p.Pro35Arg
XR_934021.1:n.211C>G
XR_934022.1:n.211C>G
XR_934023.1:n.211C>G
XM_006721516.3:c.104C>G	XP_006721579.2:p.Pro35Arg
XM_011523829.2:c.104C>G	XP_011522131.1:p.Pro35Arg
XM_011523830.2:c.104C>G	XP_011522132.1:p.Pro35Arg
XM_024450741.1:c.104C>G	XP_024306509.1:p.Pro35Arg
XR_934021.2:n.163C>G
XR_934022.2:n.163C>G
XR_934023.2:n.163C>G
NM_000018.4:c.104C>G MANE Select	NP_000009.1:p.Pro35Arg
NM_001033859.3:c.104C>G	NP_001029031.1:p.Pro35Arg
NM_001270447.2:c.173C>G	NP_001257376.1:p.Pro58Arg
NM_001270448.2:c.-125C>G	NP_001257377.1:n.-125C>G