Canonical Allele Identifier: CA397724656
Gene: ACADVL HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7127014C>G (hg19) chr17:g.7223695C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7223695C>G , CM000679.2:g.7223695C>G GRCh38
NC_000017.10:g.7127014C>G , CM000679.1:g.7127014C>G GRCh37
NC_000017.9:g.7067738C>G NCBI36
NG_007975.1:g.8862C>G
NG_008391.2:g.1356G>C
NG_033038.1:g.15850G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1234C>G MANE Select ENSP00000349297.5:p.Gln412Glu
ENST00000322910.9:c.*1189C>G ENSP00000325395.5:n.*1189C>G
ENST00000350303.9:c.1168C>G ENSP00000344152.5:p.Gln390Glu
ENST00000356839.9:c.1234C>G ENSP00000349297.5:p.Gln412Glu
ENST00000542255.6:c.92C>G
ENST00000543245.6:c.1303C>G ENSP00000438689.2:p.Gln435Glu
ENST00000578579.2:n.405C>G
ENST00000578711.1:n.191C>G
ENST00000578824.5:n.650C>G
ENST00000579425.5:n.258C>G
ENST00000579546.1:c.71C>G
ENST00000583850.5:n.9C>G
ENST00000583858.5:c.263C>G
ENST00000585203.6:n.442C>G
NM_000018.3:c.1234C>G NP_000009.1:p.Gln412Glu
NM_001033859.2:c.1168C>G NP_001029031.1:p.Gln390Glu
NM_001270447.1:c.1303C>G NP_001257376.1:p.Gln435Glu
NM_001270448.1:c.1006C>G NP_001257377.1:p.Gln336Glu
XM_006721516.2:c.1234C>G XP_006721579.2:p.Gln412Glu
XM_011523829.1:c.1234C>G XP_011522131.1:p.Gln412Glu
XM_011523830.1:c.1234C>G XP_011522132.1:p.Gln412Glu
XR_934021.1:n.1341C>G
XR_934022.1:n.1341C>G
XR_934023.1:n.1341C>G
XM_006721516.3:c.1234C>G XP_006721579.2:p.Gln412Glu
XM_011523829.2:c.1234C>G XP_011522131.1:p.Gln412Glu
XM_011523830.2:c.1234C>G XP_011522132.1:p.Gln412Glu
XM_024450741.1:c.1234C>G XP_024306509.1:p.Gln412Glu
XR_934021.2:n.1293C>G
XR_934022.2:n.1293C>G
XR_934023.2:n.1293C>G
NM_000018.4:c.1234C>G MANE Select NP_000009.1:p.Gln412Glu
NM_001033859.3:c.1168C>G NP_001029031.1:p.Gln390Glu
NM_001270447.2:c.1303C>G NP_001257376.1:p.Gln435Glu
NM_001270448.2:c.1006C>G NP_001257377.1:p.Gln336Glu
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