Canonical Allele Identifier: CA397722895

Gene: ACADVL

Linked Data

• MyVariant Identifiers: chr17:g.7124334A>T (hg19) ; chr17:g.7221015A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7221015A>T , CM000679.2:g.7221015A>T	GRCh38
NC_000017.10:g.7124334A>T , CM000679.1:g.7124334A>T	GRCh37
NC_000017.9:g.7065058A>T	NCBI36
NG_007975.1:g.6182A>T
NG_008391.2:g.4036T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.434A>T MANE Select	ENSP00000349297.5:p.Gln145Leu
ENST00000322910.9:c.*389A>T	ENSP00000325395.5:n.*389A>T
ENST00000350303.9:c.368A>T	ENSP00000344152.5:p.Gln123Leu
ENST00000356839.9:c.434A>T	ENSP00000349297.5:p.Gln145Leu
ENST00000543245.6:c.503A>T	ENSP00000438689.2:p.Gln168Leu
ENST00000577191.5:n.511A>T
ENST00000577433.5:n.642A>T
ENST00000577857.5:n.293+185A>T
ENST00000579286.5:n.615A>T
ENST00000579886.2:c.272A>T	ENSP00000463246.1:p.Gln91Leu
ENST00000580365.1:n.165A>T
ENST00000581378.5:c.133A>T
ENST00000581562.5:n.481A>T
ENST00000582056.5:n.617A>T
ENST00000582166.1:n.415A>T
ENST00000583312.5:c.434A>T	ENSP00000467920.1:p.Gln145Leu
ENST00000584103.5:c.467A>T	ENSP00000465353.1:p.Gln156Leu
NM_000018.3:c.434A>T	NP_000009.1:p.Gln145Leu
NM_001033859.2:c.368A>T	NP_001029031.1:p.Gln123Leu
NM_001270447.1:c.503A>T	NP_001257376.1:p.Gln168Leu
NM_001270448.1:c.206A>T	NP_001257377.1:p.Gln69Leu
XM_006721516.2:c.434A>T	XP_006721579.2:p.Gln145Leu
XM_011523829.1:c.434A>T	XP_011522131.1:p.Gln145Leu
XM_011523830.1:c.434A>T	XP_011522132.1:p.Gln145Leu
XR_934021.1:n.541A>T
XR_934022.1:n.541A>T
XR_934023.1:n.541A>T
XM_006721516.3:c.434A>T	XP_006721579.2:p.Gln145Leu
XM_011523829.2:c.434A>T	XP_011522131.1:p.Gln145Leu
XM_011523830.2:c.434A>T	XP_011522132.1:p.Gln145Leu
XM_024450741.1:c.434A>T	XP_024306509.1:p.Gln145Leu
XR_934021.2:n.493A>T
XR_934022.2:n.493A>T
XR_934023.2:n.493A>T
NM_000018.4:c.434A>T MANE Select	NP_000009.1:p.Gln145Leu
NM_001033859.3:c.368A>T	NP_001029031.1:p.Gln123Leu
NM_001270447.2:c.503A>T	NP_001257376.1:p.Gln168Leu
NM_001270448.2:c.206A>T	NP_001257377.1:p.Gln69Leu