Canonical Allele Identifier: CA2245699973

Gene: ACADVL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7221528_7221529delinsTC , CM000679.2:g.7221528_7221529delinsTC	GRCh38
NC_000017.10:g.7124847_7124848delinsTC , CM000679.1:g.7124847_7124848delinsTC	GRCh37
NC_000017.9:g.7065571_7065572delinsTC	NCBI36
NG_007975.1:g.6695_6696delinsTC
NG_008391.2:g.3522_3523delinsGA

Transcript Alleles

HGVS	Amino-acid change
ENST00000356839.10:c.478-10_478-9delinsTC MANE Select	ENSP00000349297.5:n.478-10_478-9delinsTC
ENST00000322910.9:c.*433-10_*433-9delinsTC	ENSP00000325395.5:n.*433-10_*433-9delinsT...
ENST00000350303.9:c.412-10_412-9delinsTC	ENSP00000344152.5:n.412-10_412-9delinsTC
ENST00000356839.9:c.478-10_478-9delinsTC	ENSP00000349297.5:n.478-10_478-9delinsTC
ENST00000543245.6:c.547-10_547-9delinsTC	ENSP00000438689.2:n.547-10_547-9delinsTC
ENST00000577191.5:n.555-10_555-9delinsTC
ENST00000577433.5:n.686-10_686-9delinsTC
ENST00000577857.5:n.294-10_294-9delinsTC
ENST00000579286.5:n.659-10_659-9delinsTC
ENST00000579886.2:c.316-10_316-9delinsTC	ENSP00000463246.1:n.316-10_316-9delinsTC
ENST00000580365.1:n.209-10_209-9delinsTC
ENST00000581378.5:c.186_187delinsTC
ENST00000581562.5:n.525-424_525-423delinsTC
ENST00000582166.1:n.459-10_459-9delinsTC
ENST00000583312.5:c.478-10_478-9delinsTC	ENSP00000467920.1:n.478-10_478-9delinsTC
ENST00000583760.1:n.250_251delinsTC
NM_000018.3:c.478-10_478-9delinsTC	NP_000009.1:n.478-10_478-9delinsTC
NM_001033859.2:c.412-10_412-9delinsTC	NP_001029031.1:n.412-10_412-9delinsTC
NM_001270447.1:c.547-10_547-9delinsTC	NP_001257376.1:n.547-10_547-9delinsTC
NM_001270448.1:c.250-10_250-9delinsTC	NP_001257377.1:n.250-10_250-9delinsTC
XM_006721516.2:c.478-10_478-9delinsTC	XP_006721579.2:n.478-10_478-9delinsTC
XM_011523829.1:c.478-10_478-9delinsTC	XP_011522131.1:n.478-10_478-9delinsTC
XM_011523830.1:c.478-10_478-9delinsTC	XP_011522132.1:n.478-10_478-9delinsTC
XR_934021.1:n.585-10_585-9delinsTC
XR_934022.1:n.585-10_585-9delinsTC
XR_934023.1:n.585-10_585-9delinsTC
XM_006721516.3:c.478-10_478-9delinsTC	XP_006721579.2:n.478-10_478-9delinsTC
XM_011523829.2:c.478-10_478-9delinsTC	XP_011522131.1:n.478-10_478-9delinsTC
XM_011523830.2:c.478-10_478-9delinsTC	XP_011522132.1:n.478-10_478-9delinsTC
XM_024450741.1:c.478-10_478-9delinsTC	XP_024306509.1:n.478-10_478-9delinsTC
XR_934021.2:n.537-10_537-9delinsTC
XR_934022.2:n.537-10_537-9delinsTC
XR_934023.2:n.537-10_537-9delinsTC
NM_000018.4:c.478-10_478-9delinsTC MANE Select	NP_000009.1:n.478-10_478-9delinsTC
NM_001033859.3:c.412-10_412-9delinsTC	NP_001029031.1:n.412-10_412-9delinsTC
NM_001270447.2:c.547-10_547-9delinsTC	NP_001257376.1:n.547-10_547-9delinsTC
NM_001270448.2:c.250-10_250-9delinsTC	NP_001257377.1:n.250-10_250-9delinsTC