Canonical Allele Identifier: CA397724183
Gene: ACADVL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222811G>C , CM000679.2:g.7222811G>C GRCh38
NC_000017.10:g.7126130G>C , CM000679.1:g.7126130G>C GRCh37
NC_000017.9:g.7066854G>C NCBI36
NG_007975.1:g.7978G>C
NG_008391.2:g.2240C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1023G>C MANE Select ENSP00000349297.5:p.Arg341Ser
ENST00000322910.9:c.*978G>C ENSP00000325395.5:n.*978G>C
ENST00000350303.9:c.957G>C ENSP00000344152.5:p.Arg319Ser
ENST00000356839.9:c.1023G>C ENSP00000349297.5:p.Arg341Ser
ENST00000543245.6:c.1092G>C ENSP00000438689.2:p.Arg364Ser
ENST00000578824.5:n.172G>C
ENST00000581378.5:c.741G>C
ENST00000582379.1:n.407G>C
ENST00000583858.5:c.52G>C
NM_000018.3:c.1023G>C NP_000009.1:p.Arg341Ser
NM_001033859.2:c.957G>C NP_001029031.1:p.Arg319Ser
NM_001270447.1:c.1092G>C NP_001257376.1:p.Arg364Ser
NM_001270448.1:c.795G>C NP_001257377.1:p.Arg265Ser
XM_006721516.2:c.1023G>C XP_006721579.2:p.Arg341Ser
XM_011523829.1:c.1023G>C XP_011522131.1:p.Arg341Ser
XM_011523830.1:c.1023G>C XP_011522132.1:p.Arg341Ser
XR_934021.1:n.1130G>C
XR_934022.1:n.1130G>C
XR_934023.1:n.1130G>C
XM_006721516.3:c.1023G>C XP_006721579.2:p.Arg341Ser
XM_011523829.2:c.1023G>C XP_011522131.1:p.Arg341Ser
XM_011523830.2:c.1023G>C XP_011522132.1:p.Arg341Ser
XM_024450741.1:c.1023G>C XP_024306509.1:p.Arg341Ser
XR_934021.2:n.1082G>C
XR_934022.2:n.1082G>C
XR_934023.2:n.1082G>C
NM_000018.4:c.1023G>C MANE Select NP_000009.1:p.Arg341Ser
NM_001033859.3:c.957G>C NP_001029031.1:p.Arg319Ser
NM_001270447.2:c.1092G>C NP_001257376.1:p.Arg364Ser
NM_001270448.2:c.795G>C NP_001257377.1:p.Arg265Ser