Canonical Allele Identifier: CA397722909
Gene: ACADVL HGNC NCBI

Linked Data

dbSNP Id: rs892944229
gnomAD v2: 17-7124342-A-G
gnomAD v3: 17-7221023-A-G
gnomAD v4: 17-7221023-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221023A>G , CM000679.2:g.7221023A>G GRCh38
NC_000017.10:g.7124342A>G , CM000679.1:g.7124342A>G GRCh37
NC_000017.9:g.7065066A>G NCBI36
NG_007975.1:g.6190A>G
NG_008391.2:g.4028T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.442A>G MANE Select ENSP00000349297.5:p.Ser148Gly
ENST00000322910.9:c.*397A>G ENSP00000325395.5:n.*397A>G
ENST00000350303.9:c.376A>G ENSP00000344152.5:p.Ser126Gly
ENST00000356839.9:c.442A>G ENSP00000349297.5:p.Ser148Gly
ENST00000543245.6:c.511A>G ENSP00000438689.2:p.Ser171Gly
ENST00000577191.5:n.519A>G
ENST00000577433.5:n.650A>G
ENST00000577857.5:n.293+193A>G
ENST00000579286.5:n.623A>G
ENST00000579886.2:c.280A>G ENSP00000463246.1:p.Ser94Gly
ENST00000580365.1:n.173A>G
ENST00000581378.5:c.141A>G
ENST00000581562.5:n.489A>G
ENST00000582056.5:n.625A>G
ENST00000582166.1:n.423A>G
ENST00000583312.5:c.442A>G ENSP00000467920.1:p.Ser148Gly
NM_000018.3:c.442A>G NP_000009.1:p.Ser148Gly
NM_001033859.2:c.376A>G NP_001029031.1:p.Ser126Gly
NM_001270447.1:c.511A>G NP_001257376.1:p.Ser171Gly
NM_001270448.1:c.214A>G NP_001257377.1:p.Ser72Gly
XM_006721516.2:c.442A>G XP_006721579.2:p.Ser148Gly
XM_011523829.1:c.442A>G XP_011522131.1:p.Ser148Gly
XM_011523830.1:c.442A>G XP_011522132.1:p.Ser148Gly
XR_934021.1:n.549A>G
XR_934022.1:n.549A>G
XR_934023.1:n.549A>G
XM_006721516.3:c.442A>G XP_006721579.2:p.Ser148Gly
XM_011523829.2:c.442A>G XP_011522131.1:p.Ser148Gly
XM_011523830.2:c.442A>G XP_011522132.1:p.Ser148Gly
XM_024450741.1:c.442A>G XP_024306509.1:p.Ser148Gly
XR_934021.2:n.501A>G
XR_934022.2:n.501A>G
XR_934023.2:n.501A>G
NM_000018.4:c.442A>G MANE Select NP_000009.1:p.Ser148Gly
NM_001033859.3:c.376A>G NP_001029031.1:p.Ser126Gly
NM_001270447.2:c.511A>G NP_001257376.1:p.Ser171Gly
NM_001270448.2:c.214A>G NP_001257377.1:p.Ser72Gly