Canonical Allele Identifier: CA1324894911
Gene: ACADL HGNC NCBI

Linked Data

dbSNP Id: rs1688953192
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.210210102C>T , CM000664.2:g.210210102C>T GRCh38
NC_000002.11:g.211074826C>T , CM000664.1:g.211074826C>T GRCh37
NC_000002.10:g.210783071C>T NCBI36
NG_008002.1:g.20390G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000233710.4:c.603+94G>A MANE Select ENSP00000233710.3:n.603+94G>A
ENST00000652584.1:n.831+94G>A
ENST00000233710.3:c.603+94G>A ENSP00000233710.3:n.603+94G>A
ENST00000482502.1:n.534G>A
NM_001608.3:c.603+94G>A NP_001599.1:n.603+94G>A
XM_005246517.3:c.540+94G>A XP_005246574.1:n.540+94G>A
XM_005246517.4:c.540+94G>A XP_005246574.1:n.540+94G>A
XM_017003955.1:c.180+94G>A XP_016859444.1:n.180+94G>A
NM_001608.4:c.603+94G>A MANE Select NP_001599.1:n.603+94G>A
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