Canonical Allele Identifier: CA2245697476

Gene: ACADVL

Linked Data

• dbSNP Id: rs2071114642

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7220076A>C , CM000679.2:g.7220076A>C	GRCh38
NC_000017.10:g.7123395A>C , CM000679.1:g.7123395A>C	GRCh37
NC_000017.9:g.7064119A>C	NCBI36
NG_007975.1:g.5243A>C
NG_008391.2:g.4975T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.62+30A>C MANE Select	ENSP00000349297.5:n.62+30A>C
ENST00000322910.9:c.92A>C	ENSP00000325395.5:p.Gln31Pro
ENST00000350303.9:c.62+30A>C	ENSP00000344152.5:n.62+30A>C
ENST00000356839.9:c.62+30A>C	ENSP00000349297.5:n.62+30A>C
ENST00000543245.6:c.132-46A>C	ENSP00000438689.2:n.132-46A>C
ENST00000577191.5:n.139+30A>C
ENST00000577857.5:n.152+30A>C
ENST00000578269.5:n.169+30A>C
ENST00000578421.1:n.151A>C
ENST00000579286.5:n.169+30A>C
ENST00000579886.2:c.62+30A>C	ENSP00000463246.1:n.62+30A>C
ENST00000580263.5:n.152+30A>C
ENST00000581562.5:n.109+30A>C
ENST00000582056.5:n.152+30A>C
ENST00000582356.5:n.187+30A>C
ENST00000583312.5:c.62+30A>C	ENSP00000467920.1:n.62+30A>C
ENST00000584103.5:c.62+30A>C	ENSP00000465353.1:n.62+30A>C
NM_000018.3:c.62+30A>C	NP_000009.1:n.62+30A>C
NM_001033859.2:c.62+30A>C	NP_001029031.1:n.62+30A>C
NM_001270447.1:c.132-46A>C	NP_001257376.1:n.132-46A>C
NM_001270448.1:c.-212A>C	NP_001257377.1:n.-212A>C
XM_006721516.2:c.62+30A>C	XP_006721579.2:n.62+30A>C
XM_011523829.1:c.62+30A>C	XP_011522131.1:n.62+30A>C
XM_011523830.1:c.62+30A>C	XP_011522132.1:n.62+30A>C
XR_934021.1:n.169+30A>C
XR_934022.1:n.169+30A>C
XR_934023.1:n.169+30A>C
XM_006721516.3:c.62+30A>C	XP_006721579.2:n.62+30A>C
XM_011523829.2:c.62+30A>C	XP_011522131.1:n.62+30A>C
XM_011523830.2:c.62+30A>C	XP_011522132.1:n.62+30A>C
XM_024450741.1:c.62+30A>C	XP_024306509.1:n.62+30A>C
XR_934021.2:n.121+30A>C
XR_934022.2:n.121+30A>C
XR_934023.2:n.121+30A>C
NM_000018.4:c.62+30A>C MANE Select	NP_000009.1:n.62+30A>C
NM_001033859.3:c.62+30A>C	NP_001029031.1:n.62+30A>C
NM_001270447.2:c.132-46A>C	NP_001257376.1:n.132-46A>C
NM_001270448.2:c.-212A>C	NP_001257377.1:n.-212A>C