Canonical Allele Identifier: CA397725436

Gene: ACADVL

Linked Data

• MyVariant Identifiers: chr17:g.7127696G>C (hg19) ; chr17:g.7224377G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7224377G>C , CM000679.2:g.7224377G>C	GRCh38
NC_000017.10:g.7127696G>C , CM000679.1:g.7127696G>C	GRCh37
NC_000017.9:g.7068420G>C	NCBI36
NG_007975.1:g.9544G>C
NG_008391.2:g.674C>G
NG_033038.1:g.15168C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.1589G>C MANE Select	ENSP00000349297.5:p.Ser530Thr
ENST00000322910.9:c.*1544G>C	ENSP00000325395.5:n.*1544G>C
ENST00000350303.9:c.1523G>C	ENSP00000344152.5:p.Ser508Thr
ENST00000356839.9:c.1589G>C	ENSP00000349297.5:p.Ser530Thr
ENST00000542255.6:c.447G>C
ENST00000543245.6:c.1658G>C	ENSP00000438689.2:p.Ser553Thr
ENST00000578319.5:n.84G>C
ENST00000578711.1:n.873G>C
ENST00000578809.5:n.161G>C
ENST00000579391.1:n.197G>C
ENST00000579425.5:n.705G>C
ENST00000579546.1:c.328G>C
ENST00000579894.5:n.376G>C
ENST00000582450.1:n.97G>C
ENST00000583074.5:n.210G>C
ENST00000583850.5:n.364G>C
ENST00000583858.5:c.520G>C
ENST00000585203.6:n.780G>C
NM_000018.3:c.1589G>C	NP_000009.1:p.Ser530Thr
NM_001033859.2:c.1523G>C	NP_001029031.1:p.Ser508Thr
NM_001270447.1:c.1658G>C	NP_001257376.1:p.Ser553Thr
NM_001270448.1:c.1361G>C	NP_001257377.1:p.Ser454Thr
XM_006721516.2:c.1589G>C	XP_006721579.2:p.Ser530Thr
XM_011523829.1:c.1491G>C	XP_011522131.1:p.Glu497Asp
XM_011523830.1:c.1491G>C	XP_011522132.1:p.Glu497Asp
XR_934021.1:n.1696G>C
XR_934022.1:n.1598G>C
XR_934023.1:n.1598G>C
XM_006721516.3:c.1589G>C	XP_006721579.2:p.Ser530Thr
XM_011523829.2:c.1491G>C	XP_011522131.1:p.Glu497Asp
XM_011523830.2:c.1491G>C	XP_011522132.1:p.Glu497Asp
XM_024450741.1:c.1491G>C	XP_024306509.1:p.Glu497Asp
XR_934021.2:n.1648G>C
XR_934022.2:n.1550G>C
XR_934023.2:n.1550G>C
NM_000018.4:c.1589G>C MANE Select	NP_000009.1:p.Ser530Thr
NM_001033859.3:c.1523G>C	NP_001029031.1:p.Ser508Thr
NM_001270447.2:c.1658G>C	NP_001257376.1:p.Ser553Thr
NM_001270448.2:c.1361G>C	NP_001257377.1:p.Ser454Thr