Canonical Allele Identifier: CA287436611

Gene: ACADVL

Linked Data

• dbSNP Id: rs1050628881
• gnomAD v4: 17-7221813-T-C
• MyVariant Identifiers: chr17:g.7125132T>C (hg19) ; chr17:g.7221813T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7221813T>C , CM000679.2:g.7221813T>C	GRCh38
NC_000017.10:g.7125132T>C , CM000679.1:g.7125132T>C	GRCh37
NC_000017.9:g.7065856T>C	NCBI36
NG_007975.1:g.6980T>C
NG_008391.2:g.3238A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000356839.10:c.622+131T>C MANE Select	ENSP00000349297.5:n.622+131T>C
ENST00000322910.9:c.*577+131T>C	ENSP00000325395.5:n.*577+131T>C
ENST00000350303.9:c.556+131T>C	ENSP00000344152.5:n.556+131T>C
ENST00000356839.9:c.622+131T>C	ENSP00000349297.5:n.622+131T>C
ENST00000543245.6:c.691+131T>C	ENSP00000438689.2:n.691+131T>C
ENST00000577191.5:n.699+131T>C
ENST00000577857.5:n.438+131T>C
ENST00000579286.5:n.803+131T>C
ENST00000579886.2:c.460+131T>C	ENSP00000463246.1:n.460+131T>C
ENST00000580365.1:n.353+131T>C
ENST00000581378.5:c.340+131T>C
ENST00000581562.5:n.525-139T>C
ENST00000583312.5:c.623-124T>C	ENSP00000467920.1:n.623-124T>C
ENST00000583760.1:n.404+131T>C
NM_000018.3:c.622+131T>C	NP_000009.1:n.622+131T>C
NM_001033859.2:c.556+131T>C	NP_001029031.1:n.556+131T>C
NM_001270447.1:c.691+131T>C	NP_001257376.1:n.691+131T>C
NM_001270448.1:c.394+131T>C	NP_001257377.1:n.394+131T>C
XM_006721516.2:c.622+131T>C	XP_006721579.2:n.622+131T>C
XM_011523829.1:c.622+131T>C	XP_011522131.1:n.622+131T>C
XM_011523830.1:c.622+131T>C	XP_011522132.1:n.622+131T>C
XR_934021.1:n.729+131T>C
XR_934022.1:n.729+131T>C
XR_934023.1:n.729+131T>C
XM_006721516.3:c.622+131T>C	XP_006721579.2:n.622+131T>C
XM_011523829.2:c.622+131T>C	XP_011522131.1:n.622+131T>C
XM_011523830.2:c.622+131T>C	XP_011522132.1:n.622+131T>C
XM_024450741.1:c.622+131T>C	XP_024306509.1:n.622+131T>C
XR_934021.2:n.681+131T>C
XR_934022.2:n.681+131T>C
XR_934023.2:n.681+131T>C
NM_000018.4:c.622+131T>C MANE Select	NP_000009.1:n.622+131T>C
NM_001033859.3:c.556+131T>C	NP_001029031.1:n.556+131T>C
NM_001270447.2:c.691+131T>C	NP_001257376.1:n.691+131T>C
NM_001270448.2:c.394+131T>C	NP_001257377.1:n.394+131T>C