Canonical Allele Identifier: CA774739971
Gene: ACADVL HGNC NCBI

Linked Data

dbSNP Id: rs1168146787
gnomAD v3: 17-7220075-C-G
gnomAD v4: 17-7220075-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7220075C>G , CM000679.2:g.7220075C>G GRCh38
NC_000017.10:g.7123394C>G , CM000679.1:g.7123394C>G GRCh37
NC_000017.9:g.7064118C>G NCBI36
NG_007975.1:g.5242C>G
NG_008391.2:g.4976G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.62+29C>G MANE Select ENSP00000349297.5:n.62+29C>G
ENST00000322910.9:c.91C>G ENSP00000325395.5:p.Gln31Glu
ENST00000350303.9:c.62+29C>G ENSP00000344152.5:n.62+29C>G
ENST00000356839.9:c.62+29C>G ENSP00000349297.5:n.62+29C>G
ENST00000543245.6:c.132-47C>G ENSP00000438689.2:n.132-47C>G
ENST00000577191.5:n.139+29C>G
ENST00000577857.5:n.152+29C>G
ENST00000578269.5:n.169+29C>G
ENST00000578421.1:n.150C>G
ENST00000579286.5:n.169+29C>G
ENST00000579886.2:c.62+29C>G ENSP00000463246.1:n.62+29C>G
ENST00000580263.5:n.152+29C>G
ENST00000581562.5:n.109+29C>G
ENST00000582056.5:n.152+29C>G
ENST00000582356.5:n.187+29C>G
ENST00000583312.5:c.62+29C>G ENSP00000467920.1:n.62+29C>G
ENST00000584103.5:c.62+29C>G ENSP00000465353.1:n.62+29C>G
NM_000018.3:c.62+29C>G NP_000009.1:n.62+29C>G
NM_001033859.2:c.62+29C>G NP_001029031.1:n.62+29C>G
NM_001270447.1:c.132-47C>G NP_001257376.1:n.132-47C>G
NM_001270448.1:c.-213C>G NP_001257377.1:n.-213C>G
XM_006721516.2:c.62+29C>G XP_006721579.2:n.62+29C>G
XM_011523829.1:c.62+29C>G XP_011522131.1:n.62+29C>G
XM_011523830.1:c.62+29C>G XP_011522132.1:n.62+29C>G
XR_934021.1:n.169+29C>G
XR_934022.1:n.169+29C>G
XR_934023.1:n.169+29C>G
XM_006721516.3:c.62+29C>G XP_006721579.2:n.62+29C>G
XM_011523829.2:c.62+29C>G XP_011522131.1:n.62+29C>G
XM_011523830.2:c.62+29C>G XP_011522132.1:n.62+29C>G
XM_024450741.1:c.62+29C>G XP_024306509.1:n.62+29C>G
XR_934021.2:n.121+29C>G
XR_934022.2:n.121+29C>G
XR_934023.2:n.121+29C>G
NM_000018.4:c.62+29C>G MANE Select NP_000009.1:n.62+29C>G
NM_001033859.3:c.62+29C>G NP_001029031.1:n.62+29C>G
NM_001270447.2:c.132-47C>G NP_001257376.1:n.132-47C>G
NM_001270448.2:c.-213C>G NP_001257377.1:n.-213C>G