Canonical Allele Identifier: CA397725121

Gene: ACADVL

Linked Data

• MyVariant Identifiers: chr17:g.7127466A>C (hg19) ; chr17:g.7224147A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7224147A>C , CM000679.2:g.7224147A>C	GRCh38
NC_000017.10:g.7127466A>C , CM000679.1:g.7127466A>C	GRCh37
NC_000017.9:g.7068190A>C	NCBI36
NG_007975.1:g.9314A>C
NG_008391.2:g.904T>G
NG_033038.1:g.15398T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000356839.10:c.1436A>C MANE Select	ENSP00000349297.5:p.Asp479Ala
ENST00000322910.9:c.*1391A>C	ENSP00000325395.5:n.*1391A>C
ENST00000350303.9:c.1370A>C	ENSP00000344152.5:p.Asp457Ala
ENST00000356839.9:c.1436A>C	ENSP00000349297.5:p.Asp479Ala
ENST00000542255.6:c.294A>C
ENST00000543245.6:c.1505A>C	ENSP00000438689.2:p.Asp502Ala
ENST00000578711.1:n.643A>C
ENST00000579391.1:n.44A>C
ENST00000579425.5:n.552A>C
ENST00000579546.1:c.271+78A>C
ENST00000579894.5:n.223A>C
ENST00000583074.5:n.153+78A>C
ENST00000583850.5:n.211A>C
ENST00000583858.5:c.463+78A>C
ENST00000585203.6:n.627A>C
NM_000018.3:c.1436A>C	NP_000009.1:p.Asp479Ala
NM_001033859.2:c.1370A>C	NP_001029031.1:p.Asp457Ala
NM_001270447.1:c.1505A>C	NP_001257376.1:p.Asp502Ala
NM_001270448.1:c.1208A>C	NP_001257377.1:p.Asp403Ala
XM_006721516.2:c.1436A>C	XP_006721579.2:p.Asp479Ala
XM_011523829.1:c.1434+78A>C	XP_011522131.1:n.1434+78A>C
XM_011523830.1:c.1434+78A>C	XP_011522132.1:n.1434+78A>C
XR_934021.1:n.1543A>C
XR_934022.1:n.1541+78A>C
XR_934023.1:n.1541+78A>C
XM_006721516.3:c.1436A>C	XP_006721579.2:p.Asp479Ala
XM_011523829.2:c.1434+78A>C	XP_011522131.1:n.1434+78A>C
XM_011523830.2:c.1434+78A>C	XP_011522132.1:n.1434+78A>C
XM_024450741.1:c.1434+78A>C	XP_024306509.1:n.1434+78A>C
XR_934021.2:n.1495A>C
XR_934022.2:n.1493+78A>C
XR_934023.2:n.1493+78A>C
NM_000018.4:c.1436A>C MANE Select	NP_000009.1:p.Asp479Ala
NM_001033859.3:c.1370A>C	NP_001029031.1:p.Asp457Ala
NM_001270447.2:c.1505A>C	NP_001257376.1:p.Asp502Ala
NM_001270448.2:c.1208A>C	NP_001257377.1:p.Asp403Ala