Canonical Allele Identifier: CA397725697

Gene: ACADVL

Linked Data

• MyVariant Identifiers: chr17:g.7127987G>C (hg19) ; chr17:g.7224668G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7224668G>C , CM000679.2:g.7224668G>C	GRCh38
NC_000017.10:g.7127987G>C , CM000679.1:g.7127987G>C	GRCh37
NC_000017.9:g.7068711G>C	NCBI36
NG_007975.1:g.9835G>C
NG_008391.2:g.383C>G
NG_033038.1:g.14877C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.1705G>C MANE Select	ENSP00000349297.5:p.Ala569Pro
ENST00000322910.9:c.*1660G>C	ENSP00000325395.5:n.*1660G>C
ENST00000350303.9:c.1639G>C	ENSP00000344152.5:p.Ala547Pro
ENST00000356839.9:c.1705G>C	ENSP00000349297.5:p.Ala569Pro
ENST00000542255.6:c.537-47G>C
ENST00000543245.6:c.1774G>C	ENSP00000438689.2:p.Ala592Pro
ENST00000578033.1:n.36G>C
ENST00000578319.5:n.286G>C
ENST00000578711.1:n.1164G>C
ENST00000578809.5:n.277G>C
ENST00000579425.5:n.821G>C
ENST00000579546.1:c.440G>C
ENST00000583074.5:n.300-47G>C
ENST00000583848.5:c.71G>C	ENSP00000466487.1:p.Gly24Ala
ENST00000583850.5:n.476G>C
ENST00000583858.5:c.636G>C
ENST00000585203.6:n.896G>C
NM_000018.3:c.1705G>C	NP_000009.1:p.Ala569Pro
NM_001033859.2:c.1639G>C	NP_001029031.1:p.Ala547Pro
NM_001270447.1:c.1774G>C	NP_001257376.1:p.Ala592Pro
NM_001270448.1:c.1477G>C	NP_001257377.1:p.Ala493Pro
XM_006721516.2:c.1679-47G>C	XP_006721579.2:n.1679-47G>C
XM_011523829.1:c.1577-47G>C	XP_011522131.1:n.1577-47G>C
XM_011523830.1:c.1603G>C	XP_011522132.1:p.Ala535Pro
XR_934021.1:n.1808G>C
XR_934022.1:n.1714G>C
XR_934023.1:n.1688-47G>C
XM_006721516.3:c.1679-47G>C	XP_006721579.2:n.1679-47G>C
XM_011523829.2:c.1577-47G>C	XP_011522131.1:n.1577-47G>C
XM_011523830.2:c.1603G>C	XP_011522132.1:p.Ala535Pro
XM_024450741.1:c.1693G>C	XP_024306509.1:p.Ala565Pro
XR_934021.2:n.1760G>C
XR_934022.2:n.1666G>C
XR_934023.2:n.1640-47G>C
NM_000018.4:c.1705G>C MANE Select	NP_000009.1:p.Ala569Pro
NM_001033859.3:c.1639G>C	NP_001029031.1:p.Ala547Pro
NM_001270447.2:c.1774G>C	NP_001257376.1:p.Ala592Pro
NM_001270448.2:c.1477G>C	NP_001257377.1:p.Ala493Pro