Canonical Allele Identifier: CA2635780685

Gene: ACADVL

Linked Data

• gnomAD v4: 17-7221202-AAACAT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7221207_7221211del , CM000679.2:g.7221207_7221211del	GRCh38
NC_000017.10:g.7124526_7124530del , CM000679.1:g.7124526_7124530del	GRCh37
NC_000017.9:g.7065250_7065254del	NCBI36
NG_007975.1:g.6374_6378del
NG_008391.2:g.3844_3848del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.477+149_477+153del MANE Select	ENSP00000349297.5:n.477+149_477+153del
ENST00000322910.9:c.*432+149_*432+153del	ENSP00000325395.5:n.*432+149_*432+153del
ENST00000350303.9:c.411+149_411+153del	ENSP00000344152.5:n.411+149_411+153del
ENST00000356839.9:c.477+149_477+153del	ENSP00000349297.5:n.477+149_477+153del
ENST00000543245.6:c.546+149_546+153del	ENSP00000438689.2:n.546+149_546+153del
ENST00000577191.5:n.554+149_554+153del
ENST00000577433.5:n.685+149_685+153del
ENST00000577857.5:n.294-331_294-327del
ENST00000579286.5:n.658+149_658+153del
ENST00000579886.2:c.315+149_315+153del	ENSP00000463246.1:n.315+149_315+153del
ENST00000580365.1:n.208+149_208+153del
ENST00000581378.5:c.176+149_176+153del
ENST00000581562.5:n.524+149_524+153del
ENST00000582166.1:n.458+149_458+153del
ENST00000583312.5:c.477+149_477+153del	ENSP00000467920.1:n.477+149_477+153del
NM_000018.3:c.477+149_477+153del	NP_000009.1:n.477+149_477+153del
NM_001033859.2:c.411+149_411+153del	NP_001029031.1:n.411+149_411+153del
NM_001270447.1:c.546+149_546+153del	NP_001257376.1:n.546+149_546+153del
NM_001270448.1:c.249+149_249+153del	NP_001257377.1:n.249+149_249+153del
XM_006721516.2:c.477+149_477+153del	XP_006721579.2:n.477+149_477+153del
XM_011523829.1:c.477+149_477+153del	XP_011522131.1:n.477+149_477+153del
XM_011523830.1:c.477+149_477+153del	XP_011522132.1:n.477+149_477+153del
XR_934021.1:n.584+149_584+153del
XR_934022.1:n.584+149_584+153del
XR_934023.1:n.584+149_584+153del
XM_006721516.3:c.477+149_477+153del	XP_006721579.2:n.477+149_477+153del
XM_011523829.2:c.477+149_477+153del	XP_011522131.1:n.477+149_477+153del
XM_011523830.2:c.477+149_477+153del	XP_011522132.1:n.477+149_477+153del
XM_024450741.1:c.477+149_477+153del	XP_024306509.1:n.477+149_477+153del
XR_934021.2:n.536+149_536+153del
XR_934022.2:n.536+149_536+153del
XR_934023.2:n.536+149_536+153del
NM_000018.4:c.477+149_477+153del MANE Select	NP_000009.1:n.477+149_477+153del
NM_001033859.3:c.411+149_411+153del	NP_001029031.1:n.411+149_411+153del
NM_001270447.2:c.546+149_546+153del	NP_001257376.1:n.546+149_546+153del
NM_001270448.2:c.249+149_249+153del	NP_001257377.1:n.249+149_249+153del