Canonical Allele Identifier: CA2245699812

Gene: ACADVL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7221434_7221435delinsAG , CM000679.2:g.7221434_7221435delinsAG	GRCh38
NC_000017.10:g.7124753_7124754delinsAG , CM000679.1:g.7124753_7124754delinsAG	GRCh37
NC_000017.9:g.7065477_7065478delinsAG	NCBI36
NG_007975.1:g.6601_6602delinsAG
NG_008391.2:g.3616_3617delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000356839.10:c.478-104_478-103delinsAG MANE Select	ENSP00000349297.5:n.478-104_478-103delins...
ENST00000322910.9:c.*433-104_*433-103delinsAG	ENSP00000325395.5:n.*433-104_*433-103deli...
ENST00000350303.9:c.412-104_412-103delinsAG	ENSP00000344152.5:n.412-104_412-103delins...
ENST00000356839.9:c.478-104_478-103delinsAG	ENSP00000349297.5:n.478-104_478-103delins...
ENST00000543245.6:c.547-104_547-103delinsAG	ENSP00000438689.2:n.547-104_547-103delins...
ENST00000577191.5:n.555-104_555-103delinsAG
ENST00000577433.5:n.686-104_686-103delinsAG
ENST00000577857.5:n.294-104_294-103delinsAG
ENST00000579286.5:n.659-104_659-103delinsAG
ENST00000579886.2:c.316-104_316-103delinsAG	ENSP00000463246.1:n.316-104_316-103delins...
ENST00000580365.1:n.209-104_209-103delinsAG
ENST00000581378.5:c.177-85_177-84delinsAG
ENST00000581562.5:n.524+376_524+377delinsAG
ENST00000582166.1:n.459-104_459-103delinsAG
ENST00000583312.5:c.478-104_478-103delinsAG	ENSP00000467920.1:n.478-104_478-103delins...
ENST00000583760.1:n.156_157delinsAG
NM_000018.3:c.478-104_478-103delinsAG	NP_000009.1:n.478-104_478-103delinsAG
NM_001033859.2:c.412-104_412-103delinsAG	NP_001029031.1:n.412-104_412-103delinsAG
NM_001270447.1:c.547-104_547-103delinsAG	NP_001257376.1:n.547-104_547-103delinsAG
NM_001270448.1:c.250-104_250-103delinsAG	NP_001257377.1:n.250-104_250-103delinsAG
XM_006721516.2:c.478-104_478-103delinsAG	XP_006721579.2:n.478-104_478-103delinsAG
XM_011523829.1:c.478-104_478-103delinsAG	XP_011522131.1:n.478-104_478-103delinsAG
XM_011523830.1:c.478-104_478-103delinsAG	XP_011522132.1:n.478-104_478-103delinsAG
XR_934021.1:n.585-104_585-103delinsAG
XR_934022.1:n.585-104_585-103delinsAG
XR_934023.1:n.585-104_585-103delinsAG
XM_006721516.3:c.478-104_478-103delinsAG	XP_006721579.2:n.478-104_478-103delinsAG
XM_011523829.2:c.478-104_478-103delinsAG	XP_011522131.1:n.478-104_478-103delinsAG
XM_011523830.2:c.478-104_478-103delinsAG	XP_011522132.1:n.478-104_478-103delinsAG
XM_024450741.1:c.478-104_478-103delinsAG	XP_024306509.1:n.478-104_478-103delinsAG
XR_934021.2:n.537-104_537-103delinsAG
XR_934022.2:n.537-104_537-103delinsAG
XR_934023.2:n.537-104_537-103delinsAG
NM_000018.4:c.478-104_478-103delinsAG MANE Select	NP_000009.1:n.478-104_478-103delinsAG
NM_001033859.3:c.412-104_412-103delinsAG	NP_001029031.1:n.412-104_412-103delinsAG
NM_001270447.2:c.547-104_547-103delinsAG	NP_001257376.1:n.547-104_547-103delinsAG
NM_001270448.2:c.250-104_250-103delinsAG	NP_001257377.1:n.250-104_250-103delinsAG