Canonical Allele Identifier: CA2662920855
Gene: ACADL HGNC NCBI

Linked Data

gnomAD v4: 2-210210095-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.210210095T>C , CM000664.2:g.210210095T>C GRCh38
NC_000002.11:g.211074819T>C , CM000664.1:g.211074819T>C GRCh37
NC_000002.10:g.210783064T>C NCBI36
NG_008002.1:g.20397A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000233710.4:c.603+101A>G MANE Select ENSP00000233710.3:n.603+101A>G
ENST00000652584.1:n.831+101A>G
ENST00000233710.3:c.603+101A>G ENSP00000233710.3:n.603+101A>G
ENST00000482502.1:n.541A>G
NM_001608.3:c.603+101A>G NP_001599.1:n.603+101A>G
XM_005246517.3:c.540+101A>G XP_005246574.1:n.540+101A>G
XM_005246517.4:c.540+101A>G XP_005246574.1:n.540+101A>G
XM_017003955.1:c.180+101A>G XP_016859444.1:n.180+101A>G
NM_001608.4:c.603+101A>G MANE Select NP_001599.1:n.603+101A>G
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