Canonical Allele Identifier: CA397722667

Gene: ACADVL

Linked Data

• MyVariant Identifiers: chr17:g.7124226T>G (hg19) ; chr17:g.7220907T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7220907T>G , CM000679.2:g.7220907T>G	GRCh38
NC_000017.10:g.7124226T>G , CM000679.1:g.7124226T>G	GRCh37
NC_000017.9:g.7064950T>G	NCBI36
NG_007975.1:g.6074T>G
NG_008391.2:g.4144A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.343-17T>G MANE Select	ENSP00000349297.5:n.343-17T>G
ENST00000322910.9:c.*298-17T>G	ENSP00000325395.5:n.*298-17T>G
ENST00000350303.9:c.277-17T>G	ENSP00000344152.5:n.277-17T>G
ENST00000356839.9:c.343-17T>G	ENSP00000349297.5:n.343-17T>G
ENST00000543245.6:c.412-17T>G	ENSP00000438689.2:n.412-17T>G
ENST00000577191.5:n.420-17T>G
ENST00000577433.5:n.551-17T>G
ENST00000577857.5:n.293+77T>G
ENST00000579286.5:n.524-17T>G
ENST00000579886.2:c.202-38T>G	ENSP00000463246.1:n.202-38T>G
ENST00000580365.1:n.74-17T>G
ENST00000581378.5:c.42-17T>G
ENST00000581562.5:n.390-17T>G
ENST00000582056.5:n.509T>G
ENST00000582166.1:n.307T>G
ENST00000582356.5:n.618T>G
ENST00000583312.5:c.343-17T>G	ENSP00000467920.1:n.343-17T>G
ENST00000584103.5:c.359T>G	ENSP00000465353.1:p.Ile120Ser
NM_000018.3:c.343-17T>G	NP_000009.1:n.343-17T>G
NM_001033859.2:c.277-17T>G	NP_001029031.1:n.277-17T>G
NM_001270447.1:c.412-17T>G	NP_001257376.1:n.412-17T>G
NM_001270448.1:c.115-17T>G	NP_001257377.1:n.115-17T>G
XM_006721516.2:c.343-17T>G	XP_006721579.2:n.343-17T>G
XM_011523829.1:c.343-17T>G	XP_011522131.1:n.343-17T>G
XM_011523830.1:c.343-17T>G	XP_011522132.1:n.343-17T>G
XR_934021.1:n.450-17T>G
XR_934022.1:n.450-17T>G
XR_934023.1:n.450-17T>G
XM_006721516.3:c.343-17T>G	XP_006721579.2:n.343-17T>G
XM_011523829.2:c.343-17T>G	XP_011522131.1:n.343-17T>G
XM_011523830.2:c.343-17T>G	XP_011522132.1:n.343-17T>G
XM_024450741.1:c.343-17T>G	XP_024306509.1:n.343-17T>G
XR_934021.2:n.402-17T>G
XR_934022.2:n.402-17T>G
XR_934023.2:n.402-17T>G
NM_000018.4:c.343-17T>G MANE Select	NP_000009.1:n.343-17T>G
NM_001033859.3:c.277-17T>G	NP_001029031.1:n.277-17T>G
NM_001270447.2:c.412-17T>G	NP_001257376.1:n.412-17T>G
NM_001270448.2:c.115-17T>G	NP_001257377.1:n.115-17T>G