Canonical Allele Identifier: CA2635786342
Gene: ACADVL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224637_7224638insGA , CM000679.2:g.7224637_7224638insGA GRCh38
NC_000017.10:g.7127956_7127957insGA , CM000679.1:g.7127956_7127957insGA GRCh37
NC_000017.9:g.7068680_7068681insGA NCBI36
NG_007975.1:g.9804_9805insGA
NG_008391.2:g.413_414insTC
NG_033038.1:g.14907_14908insTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1679-5_1679-4insGA MANE Select ENSP00000349297.5:n.1679-5_1679-4insGA
ENST00000322910.9:c.*1634-5_*1634-4insGA ENSP00000325395.5:n.*1634-5_*1634-4insGA
ENST00000350303.9:c.1613-5_1613-4insGA ENSP00000344152.5:n.1613-5_1613-4insGA
ENST00000356839.9:c.1679-5_1679-4insGA ENSP00000349297.5:n.1679-5_1679-4insGA
ENST00000542255.6:c.537-78_537-77insGA
ENST00000543245.6:c.1748-5_1748-4insGA ENSP00000438689.2:n.1748-5_1748-4insGA
ENST00000578033.1:n.5_6insGA
ENST00000578319.5:n.260-5_260-4insGA
ENST00000578711.1:n.1133_1134insGA
ENST00000578809.5:n.251-5_251-4insGA
ENST00000579425.5:n.795-5_795-4insGA
ENST00000579546.1:c.414-5_414-4insGA
ENST00000582450.1:n.271_272insGA
ENST00000583074.5:n.300-78_300-77insGA
ENST00000583848.5:c.65-25_65-24insGA ENSP00000466487.1:n.65-25_65-24insGA
ENST00000583850.5:n.450-5_450-4insGA
ENST00000583858.5:c.610-5_610-4insGA
ENST00000585203.6:n.870-5_870-4insGA
NM_000018.3:c.1679-5_1679-4insGA NP_000009.1:n.1679-5_1679-4insGA
NM_001033859.2:c.1613-5_1613-4insGA NP_001029031.1:n.1613-5_1613-4insGA
NM_001270447.1:c.1748-5_1748-4insGA NP_001257376.1:n.1748-5_1748-4insGA
NM_001270448.1:c.1451-5_1451-4insGA NP_001257377.1:n.1451-5_1451-4insGA
XM_006721516.2:c.1679-78_1679-77insGA XP_006721579.2:n.1679-78_1679-77insGA
XM_011523829.1:c.1577-78_1577-77insGA XP_011522131.1:n.1577-78_1577-77insGA
XM_011523830.1:c.1577-5_1577-4insGA XP_011522132.1:n.1577-5_1577-4insGA
XR_934021.1:n.1782-5_1782-4insGA
XR_934022.1:n.1688-5_1688-4insGA
XR_934023.1:n.1688-78_1688-77insGA
XM_006721516.3:c.1679-78_1679-77insGA XP_006721579.2:n.1679-78_1679-77insGA
XM_011523829.2:c.1577-78_1577-77insGA XP_011522131.1:n.1577-78_1577-77insGA
XM_011523830.2:c.1577-5_1577-4insGA XP_011522132.1:n.1577-5_1577-4insGA
XM_024450741.1:c.1667-5_1667-4insGA XP_024306509.1:n.1667-5_1667-4insGA
XR_934021.2:n.1734-5_1734-4insGA
XR_934022.2:n.1640-5_1640-4insGA
XR_934023.2:n.1640-78_1640-77insGA
NM_000018.4:c.1679-5_1679-4insGA MANE Select NP_000009.1:n.1679-5_1679-4insGA
NM_001033859.3:c.1613-5_1613-4insGA NP_001029031.1:n.1613-5_1613-4insGA
NM_001270447.2:c.1748-5_1748-4insGA NP_001257376.1:n.1748-5_1748-4insGA
NM_001270448.2:c.1451-5_1451-4insGA NP_001257377.1:n.1451-5_1451-4insGA