Canonical Allele Identifier: CA913186028

Gene: ACADVL

Linked Data

• gnomAD v4: 17-7220688-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7220688G>C , CM000679.2:g.7220688G>C	GRCh38
NC_000017.10:g.7124007G>C , CM000679.1:g.7124007G>C	GRCh37
NC_000017.9:g.7064731G>C	NCBI36
NG_007975.1:g.5855G>C
NG_008391.2:g.4363C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.277+12G>C MANE Select	ENSP00000349297.5:n.277+12G>C
ENST00000322910.9:c.*232+12G>C	ENSP00000325395.5:n.*232+12G>C
ENST00000350303.9:c.211+12G>C	ENSP00000344152.5:n.211+12G>C
ENST00000356839.9:c.277+12G>C	ENSP00000349297.5:n.277+12G>C
ENST00000543245.6:c.346+12G>C	ENSP00000438689.2:n.346+12G>C
ENST00000577191.5:n.354+12G>C
ENST00000577433.5:n.485+12G>C
ENST00000577857.5:n.229-78G>C
ENST00000578421.1:n.497G>C
ENST00000579286.5:n.458+12G>C
ENST00000579886.2:c.201+162G>C	ENSP00000463246.1:n.201+162G>C
ENST00000580263.5:n.453G>C
ENST00000581562.5:n.324+12G>C
ENST00000582056.5:n.367+12G>C
ENST00000582166.1:n.165+12G>C
ENST00000582356.5:n.476+12G>C
ENST00000583312.5:c.277+12G>C	ENSP00000467920.1:n.277+12G>C
ENST00000584103.5:c.277+12G>C	ENSP00000465353.1:n.277+12G>C
NM_000018.3:c.277+12G>C	NP_000009.1:n.277+12G>C
NM_001033859.2:c.211+12G>C	NP_001029031.1:n.211+12G>C
NM_001270447.1:c.346+12G>C	NP_001257376.1:n.346+12G>C
NM_001270448.1:c.49+12G>C	NP_001257377.1:n.49+12G>C
XM_006721516.2:c.277+12G>C	XP_006721579.2:n.277+12G>C
XM_011523829.1:c.277+12G>C	XP_011522131.1:n.277+12G>C
XM_011523830.1:c.277+12G>C	XP_011522132.1:n.277+12G>C
XR_934021.1:n.384+12G>C
XR_934022.1:n.384+12G>C
XR_934023.1:n.384+12G>C
XM_006721516.3:c.277+12G>C	XP_006721579.2:n.277+12G>C
XM_011523829.2:c.277+12G>C	XP_011522131.1:n.277+12G>C
XM_011523830.2:c.277+12G>C	XP_011522132.1:n.277+12G>C
XM_024450741.1:c.277+12G>C	XP_024306509.1:n.277+12G>C
XR_934021.2:n.336+12G>C
XR_934022.2:n.336+12G>C
XR_934023.2:n.336+12G>C
NM_000018.4:c.277+12G>C MANE Select	NP_000009.1:n.277+12G>C
NM_001033859.3:c.211+12G>C	NP_001029031.1:n.211+12G>C
NM_001270447.2:c.346+12G>C	NP_001257376.1:n.346+12G>C
NM_001270448.2:c.49+12G>C	NP_001257377.1:n.49+12G>C