Canonical Allele Identifier: CA2841827553

Gene: ACADVL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7224407G>T , CM000679.2:g.7224407G>T	GRCh38
NC_000017.10:g.7127726G>T , CM000679.1:g.7127726G>T	GRCh37
NC_000017.9:g.7068450G>T	NCBI36
NG_007975.1:g.9574G>T
NG_008391.2:g.644C>A
NG_033038.1:g.15138C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.1605+14G>T MANE Select	ENSP00000349297.5:n.1605+14G>T
ENST00000322910.9:c.*1560+14G>T	ENSP00000325395.5:n.*1560+14G>T
ENST00000350303.9:c.1539+14G>T	ENSP00000344152.5:n.1539+14G>T
ENST00000356839.9:c.1605+14G>T	ENSP00000349297.5:n.1605+14G>T
ENST00000542255.6:c.463+14G>T
ENST00000543245.6:c.1674+14G>T	ENSP00000438689.2:n.1674+14G>T
ENST00000578319.5:n.114G>T
ENST00000578711.1:n.903G>T
ENST00000578809.5:n.177+14G>T
ENST00000579391.1:n.213+14G>T
ENST00000579425.5:n.721+14G>T
ENST00000579546.1:c.344+14G>T
ENST00000579894.5:n.392+14G>T
ENST00000582450.1:n.113+14G>T
ENST00000583074.5:n.226+14G>T
ENST00000583850.5:n.380+14G>T
ENST00000583858.5:c.536+14G>T
ENST00000585203.6:n.796+14G>T
NM_000018.3:c.1605+14G>T	NP_000009.1:n.1605+14G>T
NM_001033859.2:c.1539+14G>T	NP_001029031.1:n.1539+14G>T
NM_001270447.1:c.1674+14G>T	NP_001257376.1:n.1674+14G>T
NM_001270448.1:c.1377+14G>T	NP_001257377.1:n.1377+14G>T
XM_006721516.2:c.1605+14G>T	XP_006721579.2:n.1605+14G>T
XM_011523829.1:c.1507+14G>T	XP_011522131.1:n.1507+14G>T
XM_011523830.1:c.1507+14G>T	XP_011522132.1:n.1507+14G>T
XR_934021.1:n.1712+14G>T
XR_934022.1:n.1614+14G>T
XR_934023.1:n.1614+14G>T
XM_006721516.3:c.1605+14G>T	XP_006721579.2:n.1605+14G>T
XM_011523829.2:c.1507+14G>T	XP_011522131.1:n.1507+14G>T
XM_011523830.2:c.1507+14G>T	XP_011522132.1:n.1507+14G>T
XM_024450741.1:c.1521G>T	XP_024306509.1:p.Gly507=
XR_934021.2:n.1664+14G>T
XR_934022.2:n.1566+14G>T
XR_934023.2:n.1566+14G>T
NM_000018.4:c.1605+14G>T MANE Select	NP_000009.1:n.1605+14G>T
NM_001033859.3:c.1539+14G>T	NP_001029031.1:n.1539+14G>T
NM_001270447.2:c.1674+14G>T	NP_001257376.1:n.1674+14G>T
NM_001270448.2:c.1377+14G>T	NP_001257377.1:n.1377+14G>T