Canonical Allele Identifier: CA397723099

Gene: ACADVL

Linked Data

• MyVariant Identifiers: chr17:g.7124908A>C (hg19) ; chr17:g.7221589A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7221589A>C , CM000679.2:g.7221589A>C	GRCh38
NC_000017.10:g.7124908A>C , CM000679.1:g.7124908A>C	GRCh37
NC_000017.9:g.7065632A>C	NCBI36
NG_007975.1:g.6756A>C
NG_008391.2:g.3462T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000356839.10:c.529A>C MANE Select	ENSP00000349297.5:p.Thr177Pro
ENST00000322910.9:c.*484A>C	ENSP00000325395.5:n.*484A>C
ENST00000350303.9:c.463A>C	ENSP00000344152.5:p.Thr155Pro
ENST00000356839.9:c.529A>C	ENSP00000349297.5:p.Thr177Pro
ENST00000543245.6:c.598A>C	ENSP00000438689.2:p.Thr200Pro
ENST00000577191.5:n.606A>C
ENST00000577433.5:n.737A>C
ENST00000577857.5:n.345A>C
ENST00000579286.5:n.710A>C
ENST00000579886.2:c.367A>C	ENSP00000463246.1:p.Thr123Pro
ENST00000580365.1:n.260A>C
ENST00000581378.5:c.247A>C
ENST00000581562.5:n.525-363A>C
ENST00000582166.1:n.510A>C
ENST00000583312.5:c.529A>C	ENSP00000467920.1:p.Thr177Pro
ENST00000583760.1:n.311A>C
NM_000018.3:c.529A>C	NP_000009.1:p.Thr177Pro
NM_001033859.2:c.463A>C	NP_001029031.1:p.Thr155Pro
NM_001270447.1:c.598A>C	NP_001257376.1:p.Thr200Pro
NM_001270448.1:c.301A>C	NP_001257377.1:p.Thr101Pro
XM_006721516.2:c.529A>C	XP_006721579.2:p.Thr177Pro
XM_011523829.1:c.529A>C	XP_011522131.1:p.Thr177Pro
XM_011523830.1:c.529A>C	XP_011522132.1:p.Thr177Pro
XR_934021.1:n.636A>C
XR_934022.1:n.636A>C
XR_934023.1:n.636A>C
XM_006721516.3:c.529A>C	XP_006721579.2:p.Thr177Pro
XM_011523829.2:c.529A>C	XP_011522131.1:p.Thr177Pro
XM_011523830.2:c.529A>C	XP_011522132.1:p.Thr177Pro
XM_024450741.1:c.529A>C	XP_024306509.1:p.Thr177Pro
XR_934021.2:n.588A>C
XR_934022.2:n.588A>C
XR_934023.2:n.588A>C
NM_000018.4:c.529A>C MANE Select	NP_000009.1:p.Thr177Pro
NM_001033859.3:c.463A>C	NP_001029031.1:p.Thr155Pro
NM_001270447.2:c.598A>C	NP_001257376.1:p.Thr200Pro
NM_001270448.2:c.301A>C	NP_001257377.1:p.Thr101Pro