Canonical Allele Identifier: CA397722057

Gene: ACADVL

Linked Data

• gnomAD v4: 17-7220142-T-C
• MyVariant Identifiers: chr17:g.7123461T>C (hg19) ; chr17:g.7220142T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7220142T>C , CM000679.2:g.7220142T>C	GRCh38
NC_000017.10:g.7123461T>C , CM000679.1:g.7123461T>C	GRCh37
NC_000017.9:g.7064185T>C	NCBI36
NG_007975.1:g.5309T>C
NG_008391.2:g.4909A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.83T>C MANE Select	ENSP00000349297.5:p.Leu28Pro
ENST00000322910.9:c.*38T>C	ENSP00000325395.5:n.*38T>C
ENST00000350303.9:c.83T>C	ENSP00000344152.5:p.Leu28Pro
ENST00000356839.9:c.83T>C	ENSP00000349297.5:p.Leu28Pro
ENST00000543245.6:c.152T>C	ENSP00000438689.2:p.Leu51Pro
ENST00000577191.5:n.160T>C
ENST00000577857.5:n.173T>C
ENST00000578269.5:n.190T>C
ENST00000578421.1:n.217T>C
ENST00000579286.5:n.190T>C
ENST00000579886.2:c.83T>C	ENSP00000463246.1:p.Leu28Pro
ENST00000580263.5:n.173T>C
ENST00000581562.5:n.130T>C
ENST00000582056.5:n.173T>C
ENST00000582356.5:n.208T>C
ENST00000583312.5:c.83T>C	ENSP00000467920.1:p.Leu28Pro
ENST00000584103.5:c.83T>C	ENSP00000465353.1:p.Leu28Pro
NM_000018.3:c.83T>C	NP_000009.1:p.Leu28Pro
NM_001033859.2:c.83T>C	NP_001029031.1:p.Leu28Pro
NM_001270447.1:c.152T>C	NP_001257376.1:p.Leu51Pro
NM_001270448.1:c.-146T>C	NP_001257377.1:n.-146T>C
XM_006721516.2:c.83T>C	XP_006721579.2:p.Leu28Pro
XM_011523829.1:c.83T>C	XP_011522131.1:p.Leu28Pro
XM_011523830.1:c.83T>C	XP_011522132.1:p.Leu28Pro
XR_934021.1:n.190T>C
XR_934022.1:n.190T>C
XR_934023.1:n.190T>C
XM_006721516.3:c.83T>C	XP_006721579.2:p.Leu28Pro
XM_011523829.2:c.83T>C	XP_011522131.1:p.Leu28Pro
XM_011523830.2:c.83T>C	XP_011522132.1:p.Leu28Pro
XM_024450741.1:c.83T>C	XP_024306509.1:p.Leu28Pro
XR_934021.2:n.142T>C
XR_934022.2:n.142T>C
XR_934023.2:n.142T>C
NM_000018.4:c.83T>C MANE Select	NP_000009.1:p.Leu28Pro
NM_001033859.3:c.83T>C	NP_001029031.1:p.Leu28Pro
NM_001270447.2:c.152T>C	NP_001257376.1:p.Leu51Pro
NM_001270448.2:c.-146T>C	NP_001257377.1:n.-146T>C