Canonical Allele Identifier: CA397722783

Gene: ACADVL

Linked Data

• MyVariant Identifiers: chr17:g.7124281G>C (hg19) ; chr17:g.7220962G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7220962G>C , CM000679.2:g.7220962G>C	GRCh38
NC_000017.10:g.7124281G>C , CM000679.1:g.7124281G>C	GRCh37
NC_000017.9:g.7065005G>C	NCBI36
NG_007975.1:g.6129G>C
NG_008391.2:g.4089C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.381G>C MANE Select	ENSP00000349297.5:p.Met127Ile
ENST00000322910.9:c.*336G>C	ENSP00000325395.5:n.*336G>C
ENST00000350303.9:c.315G>C	ENSP00000344152.5:p.Met105Ile
ENST00000356839.9:c.381G>C	ENSP00000349297.5:p.Met127Ile
ENST00000543245.6:c.450G>C	ENSP00000438689.2:p.Met150Ile
ENST00000577191.5:n.458G>C
ENST00000577433.5:n.589G>C
ENST00000577857.5:n.293+132G>C
ENST00000579286.5:n.562G>C
ENST00000579886.2:c.219G>C	ENSP00000463246.1:p.Met73Ile
ENST00000580365.1:n.112G>C
ENST00000581378.5:c.80G>C
ENST00000581562.5:n.428G>C
ENST00000582056.5:n.564G>C
ENST00000582166.1:n.362G>C
ENST00000583312.5:c.381G>C	ENSP00000467920.1:p.Met127Ile
ENST00000584103.5:c.414G>C	ENSP00000465353.1:p.Met138Ile
NM_000018.3:c.381G>C	NP_000009.1:p.Met127Ile
NM_001033859.2:c.315G>C	NP_001029031.1:p.Met105Ile
NM_001270447.1:c.450G>C	NP_001257376.1:p.Met150Ile
NM_001270448.1:c.153G>C	NP_001257377.1:p.Met51Ile
XM_006721516.2:c.381G>C	XP_006721579.2:p.Met127Ile
XM_011523829.1:c.381G>C	XP_011522131.1:p.Met127Ile
XM_011523830.1:c.381G>C	XP_011522132.1:p.Met127Ile
XR_934021.1:n.488G>C
XR_934022.1:n.488G>C
XR_934023.1:n.488G>C
XM_006721516.3:c.381G>C	XP_006721579.2:p.Met127Ile
XM_011523829.2:c.381G>C	XP_011522131.1:p.Met127Ile
XM_011523830.2:c.381G>C	XP_011522132.1:p.Met127Ile
XM_024450741.1:c.381G>C	XP_024306509.1:p.Met127Ile
XR_934021.2:n.440G>C
XR_934022.2:n.440G>C
XR_934023.2:n.440G>C
NM_000018.4:c.381G>C MANE Select	NP_000009.1:p.Met127Ile
NM_001033859.3:c.315G>C	NP_001029031.1:p.Met105Ile
NM_001270447.2:c.450G>C	NP_001257376.1:p.Met150Ile
NM_001270448.2:c.153G>C	NP_001257377.1:p.Met51Ile