Canonical Allele Identifier: CA397725487

Gene: ACADVL

Linked Data

• MyVariant Identifiers: chr17:g.7127802G>C (hg19) ; chr17:g.7224483G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7224483G>C , CM000679.2:g.7224483G>C	GRCh38
NC_000017.10:g.7127802G>C , CM000679.1:g.7127802G>C	GRCh37
NC_000017.9:g.7068526G>C	NCBI36
NG_007975.1:g.9650G>C
NG_008391.2:g.568C>G
NG_033038.1:g.15062C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000356839.10:c.1609G>C MANE Select	ENSP00000349297.5:p.Val537Leu
ENST00000322910.9:c.*1564G>C	ENSP00000325395.5:n.*1564G>C
ENST00000350303.9:c.1543G>C	ENSP00000344152.5:p.Val515Leu
ENST00000356839.9:c.1609G>C	ENSP00000349297.5:p.Val537Leu
ENST00000542255.6:c.467G>C
ENST00000543245.6:c.1678G>C	ENSP00000438689.2:p.Val560Leu
ENST00000578319.5:n.190G>C
ENST00000578711.1:n.979G>C
ENST00000578809.5:n.181G>C
ENST00000579391.1:n.214-1G>C
ENST00000579425.5:n.725G>C
ENST00000579546.1:c.345-1G>C
ENST00000579894.5:n.396G>C
ENST00000582450.1:n.117G>C
ENST00000583074.5:n.230G>C
ENST00000583850.5:n.381-1G>C
ENST00000583858.5:c.540G>C
ENST00000585203.6:n.800G>C
NM_000018.3:c.1609G>C	NP_000009.1:p.Val537Leu
NM_001033859.2:c.1543G>C	NP_001029031.1:p.Val515Leu
NM_001270447.1:c.1678G>C	NP_001257376.1:p.Val560Leu
NM_001270448.1:c.1381G>C	NP_001257377.1:p.Val461Leu
XM_006721516.2:c.1609G>C	XP_006721579.2:p.Val537Leu
XM_011523829.1:c.1508-1G>C	XP_011522131.1:n.1508-1G>C
XM_011523830.1:c.1508-1G>C	XP_011522132.1:n.1508-1G>C
XR_934021.1:n.1713-1G>C
XR_934022.1:n.1618G>C
XR_934023.1:n.1618G>C
XM_006721516.3:c.1609G>C	XP_006721579.2:p.Val537Leu
XM_011523829.2:c.1508-1G>C	XP_011522131.1:n.1508-1G>C
XM_011523830.2:c.1508-1G>C	XP_011522132.1:n.1508-1G>C
XM_024450741.1:c.1597G>C	XP_024306509.1:p.Val533Leu
XR_934021.2:n.1665-1G>C
XR_934022.2:n.1570G>C
XR_934023.2:n.1570G>C
NM_000018.4:c.1609G>C MANE Select	NP_000009.1:p.Val537Leu
NM_001033859.3:c.1543G>C	NP_001029031.1:p.Val515Leu
NM_001270447.2:c.1678G>C	NP_001257376.1:p.Val560Leu
NM_001270448.2:c.1381G>C	NP_001257377.1:p.Val461Leu