Canonical Allele Identifier: CA2635779923

Gene: ACADVL

Linked Data

• gnomAD v4: 17-7220381-CCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7220383_7220384del , CM000679.2:g.7220383_7220384del	GRCh38
NC_000017.10:g.7123702_7123703del , CM000679.1:g.7123702_7123703del	GRCh37
NC_000017.9:g.7064426_7064427del	NCBI36
NG_007975.1:g.5550_5551del
NG_008391.2:g.4668_4669del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.139-81_139-80del MANE Select	ENSP00000349297.5:n.139-81_139-80del
ENST00000322910.9:c.*94-81_*94-80del	ENSP00000325395.5:n.*94-81_*94-80del
ENST00000350303.9:c.138+186_138+187del	ENSP00000344152.5:n.138+186_138+187del
ENST00000356839.9:c.139-81_139-80del	ENSP00000349297.5:n.139-81_139-80del
ENST00000543245.6:c.208-81_208-80del	ENSP00000438689.2:n.208-81_208-80del
ENST00000577191.5:n.216-81_216-80del
ENST00000577433.5:n.192_193del
ENST00000577857.5:n.228+186_228+187del
ENST00000578269.5:n.431_432del
ENST00000578421.1:n.273-81_273-80del
ENST00000579286.5:n.246-81_246-80del
ENST00000579886.2:c.139-81_139-80del	ENSP00000463246.1:n.139-81_139-80del
ENST00000580263.5:n.229-81_229-80del
ENST00000581562.5:n.186-81_186-80del
ENST00000582056.5:n.229-81_229-80del
ENST00000582356.5:n.264-81_264-80del
ENST00000583312.5:c.139-81_139-80del	ENSP00000467920.1:n.139-81_139-80del
ENST00000584103.5:c.139-81_139-80del	ENSP00000465353.1:n.139-81_139-80del
NM_000018.3:c.139-81_139-80del	NP_000009.1:n.139-81_139-80del
NM_001033859.2:c.138+186_138+187del	NP_001029031.1:n.138+186_138+187del
NM_001270447.1:c.208-81_208-80del	NP_001257376.1:n.208-81_208-80del
NM_001270448.1:c.-90-81_-90-80del	NP_001257377.1:n.-90-81_-90-80del
XM_006721516.2:c.139-81_139-80del	XP_006721579.2:n.139-81_139-80del
XM_011523829.1:c.139-81_139-80del	XP_011522131.1:n.139-81_139-80del
XM_011523830.1:c.139-81_139-80del	XP_011522132.1:n.139-81_139-80del
XR_934021.1:n.246-81_246-80del
XR_934022.1:n.246-81_246-80del
XR_934023.1:n.246-81_246-80del
XM_006721516.3:c.139-81_139-80del	XP_006721579.2:n.139-81_139-80del
XM_011523829.2:c.139-81_139-80del	XP_011522131.1:n.139-81_139-80del
XM_011523830.2:c.139-81_139-80del	XP_011522132.1:n.139-81_139-80del
XM_024450741.1:c.139-81_139-80del	XP_024306509.1:n.139-81_139-80del
XR_934021.2:n.198-81_198-80del
XR_934022.2:n.198-81_198-80del
XR_934023.2:n.198-81_198-80del
NM_000018.4:c.139-81_139-80del MANE Select	NP_000009.1:n.139-81_139-80del
NM_001033859.3:c.138+186_138+187del	NP_001029031.1:n.138+186_138+187del
NM_001270447.2:c.208-81_208-80del	NP_001257376.1:n.208-81_208-80del
NM_001270448.2:c.-90-81_-90-80del	NP_001257377.1:n.-90-81_-90-80del