Canonical Allele Identifier: CA397722439

Gene: ACADVL

Linked Data

• MyVariant Identifiers: chr17:g.7123976G>C (hg19) ; chr17:g.7220657G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7220657G>C , CM000679.2:g.7220657G>C	GRCh38
NC_000017.10:g.7123976G>C , CM000679.1:g.7123976G>C	GRCh37
NC_000017.9:g.7064700G>C	NCBI36
NG_007975.1:g.5824G>C
NG_008391.2:g.4394C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.258G>C MANE Select	ENSP00000349297.5:p.Gln86His
ENST00000322910.9:c.*213G>C	ENSP00000325395.5:n.*213G>C
ENST00000350303.9:c.192G>C	ENSP00000344152.5:p.Gln64His
ENST00000356839.9:c.258G>C	ENSP00000349297.5:p.Gln86His
ENST00000543245.6:c.327G>C	ENSP00000438689.2:p.Gln109His
ENST00000577191.5:n.335G>C
ENST00000577433.5:n.466G>C
ENST00000577857.5:n.229-109G>C
ENST00000578269.5:n.705G>C
ENST00000578421.1:n.466G>C
ENST00000579286.5:n.439G>C
ENST00000579886.2:c.201+131G>C	ENSP00000463246.1:n.201+131G>C
ENST00000580263.5:n.422G>C
ENST00000581562.5:n.305G>C
ENST00000582056.5:n.348G>C
ENST00000582166.1:n.146G>C
ENST00000582356.5:n.457G>C
ENST00000583312.5:c.258G>C	ENSP00000467920.1:p.Gln86His
ENST00000584103.5:c.258G>C	ENSP00000465353.1:p.Gln86His
NM_000018.3:c.258G>C	NP_000009.1:p.Gln86His
NM_001033859.2:c.192G>C	NP_001029031.1:p.Gln64His
NM_001270447.1:c.327G>C	NP_001257376.1:p.Gln109His
NM_001270448.1:c.30G>C	NP_001257377.1:p.Gln10His
XM_006721516.2:c.258G>C	XP_006721579.2:p.Gln86His
XM_011523829.1:c.258G>C	XP_011522131.1:p.Gln86His
XM_011523830.1:c.258G>C	XP_011522132.1:p.Gln86His
XR_934021.1:n.365G>C
XR_934022.1:n.365G>C
XR_934023.1:n.365G>C
XM_006721516.3:c.258G>C	XP_006721579.2:p.Gln86His
XM_011523829.2:c.258G>C	XP_011522131.1:p.Gln86His
XM_011523830.2:c.258G>C	XP_011522132.1:p.Gln86His
XM_024450741.1:c.258G>C	XP_024306509.1:p.Gln86His
XR_934021.2:n.317G>C
XR_934022.2:n.317G>C
XR_934023.2:n.317G>C
NM_000018.4:c.258G>C MANE Select	NP_000009.1:p.Gln86His
NM_001033859.3:c.192G>C	NP_001029031.1:p.Gln64His
NM_001270447.2:c.327G>C	NP_001257376.1:p.Gln109His
NM_001270448.2:c.30G>C	NP_001257377.1:p.Gln10His