Canonical Allele Identifier: CA397725590
Gene: ACADVL HGNC NCBI

Linked Data

dbSNP Id: rs1433810416
gnomAD v3: 17-7224535-A-C
gnomAD v4: 17-7224535-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224535A>C , CM000679.2:g.7224535A>C GRCh38
NC_000017.10:g.7127854A>C , CM000679.1:g.7127854A>C GRCh37
NC_000017.9:g.7068578A>C NCBI36
NG_007975.1:g.9702A>C
NG_008391.2:g.516T>G
NG_033038.1:g.15010T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1661A>C MANE Select ENSP00000349297.5:p.His554Pro
ENST00000322910.9:c.*1616A>C ENSP00000325395.5:n.*1616A>C
ENST00000350303.9:c.1595A>C ENSP00000344152.5:p.His532Pro
ENST00000356839.9:c.1661A>C ENSP00000349297.5:p.His554Pro
ENST00000542255.6:c.519A>C
ENST00000543245.6:c.1730A>C ENSP00000438689.2:p.His577Pro
ENST00000578319.5:n.242A>C
ENST00000578711.1:n.1031A>C
ENST00000578809.5:n.233A>C
ENST00000579391.1:n.265A>C
ENST00000579425.5:n.777A>C
ENST00000579546.1:c.396A>C
ENST00000582450.1:n.169A>C
ENST00000583074.5:n.282A>C
ENST00000583848.5:c.47A>C ENSP00000466487.1:p.His16Pro
ENST00000583850.5:n.432A>C
ENST00000583858.5:c.592A>C
ENST00000585203.6:n.852A>C
NM_000018.3:c.1661A>C NP_000009.1:p.His554Pro
NM_001033859.2:c.1595A>C NP_001029031.1:p.His532Pro
NM_001270447.1:c.1730A>C NP_001257376.1:p.His577Pro
NM_001270448.1:c.1433A>C NP_001257377.1:p.His478Pro
XM_006721516.2:c.1661A>C XP_006721579.2:p.His554Pro
XM_011523829.1:c.1559A>C XP_011522131.1:p.His520Pro
XM_011523830.1:c.1559A>C XP_011522132.1:p.His520Pro
XR_934021.1:n.1764A>C
XR_934022.1:n.1670A>C
XR_934023.1:n.1670A>C
XM_006721516.3:c.1661A>C XP_006721579.2:p.His554Pro
XM_011523829.2:c.1559A>C XP_011522131.1:p.His520Pro
XM_011523830.2:c.1559A>C XP_011522132.1:p.His520Pro
XM_024450741.1:c.1649A>C XP_024306509.1:p.His550Pro
XR_934021.2:n.1716A>C
XR_934022.2:n.1622A>C
XR_934023.2:n.1622A>C
NM_000018.4:c.1661A>C MANE Select NP_000009.1:p.His554Pro
NM_001033859.3:c.1595A>C NP_001029031.1:p.His532Pro
NM_001270447.2:c.1730A>C NP_001257376.1:p.His577Pro
NM_001270448.2:c.1433A>C NP_001257377.1:p.His478Pro