Canonical Allele Identifier: CA397725771

Gene: ACADVL

Linked Data

• MyVariant Identifiers: chr17:g.7128021T>C (hg19) ; chr17:g.7224702T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7224702T>C , CM000679.2:g.7224702T>C	GRCh38
NC_000017.10:g.7128021T>C , CM000679.1:g.7128021T>C	GRCh37
NC_000017.9:g.7068745T>C	NCBI36
NG_007975.1:g.9869T>C
NG_008391.2:g.349A>G
NG_033038.1:g.14843A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000356839.10:c.1739T>C MANE Select	ENSP00000349297.5:p.Val580Ala
ENST00000322910.9:c.*1694T>C	ENSP00000325395.5:n.*1694T>C
ENST00000350303.9:c.1673T>C	ENSP00000344152.5:p.Val558Ala
ENST00000356839.9:c.1739T>C	ENSP00000349297.5:p.Val580Ala
ENST00000542255.6:c.537-13T>C
ENST00000543245.6:c.1808T>C	ENSP00000438689.2:p.Val603Ala
ENST00000578033.1:n.70T>C
ENST00000578319.5:n.320T>C
ENST00000578711.1:n.1198T>C
ENST00000578809.5:n.311T>C
ENST00000579425.5:n.855T>C
ENST00000579546.1:c.474T>C
ENST00000583074.5:n.300-13T>C
ENST00000583848.5:c.105T>C	ENSP00000466487.1:p.Gly35=
ENST00000583850.5:n.510T>C
ENST00000583858.5:c.670T>C
ENST00000585203.6:n.930T>C
NM_000018.3:c.1739T>C	NP_000009.1:p.Val580Ala
NM_001033859.2:c.1673T>C	NP_001029031.1:p.Val558Ala
NM_001270447.1:c.1808T>C	NP_001257376.1:p.Val603Ala
NM_001270448.1:c.1511T>C	NP_001257377.1:p.Val504Ala
XM_006721516.2:c.1679-13T>C	XP_006721579.2:n.1679-13T>C
XM_011523829.1:c.1577-13T>C	XP_011522131.1:n.1577-13T>C
XM_011523830.1:c.1637T>C	XP_011522132.1:p.Val546Ala
XR_934021.1:n.1842T>C
XR_934022.1:n.1748T>C
XR_934023.1:n.1688-13T>C
XM_006721516.3:c.1679-13T>C	XP_006721579.2:n.1679-13T>C
XM_011523829.2:c.1577-13T>C	XP_011522131.1:n.1577-13T>C
XM_011523830.2:c.1637T>C	XP_011522132.1:p.Val546Ala
XM_024450741.1:c.1727T>C	XP_024306509.1:p.Val576Ala
XR_934021.2:n.1794T>C
XR_934022.2:n.1700T>C
XR_934023.2:n.1640-13T>C
NM_000018.4:c.1739T>C MANE Select	NP_000009.1:p.Val580Ala
NM_001033859.3:c.1673T>C	NP_001029031.1:p.Val558Ala
NM_001270447.2:c.1808T>C	NP_001257376.1:p.Val603Ala
NM_001270448.2:c.1511T>C	NP_001257377.1:p.Val504Ala