Canonical Allele Identifier: CA1324894903
Gene: ACADL HGNC NCBI

Linked Data

dbSNP Id: rs1688952839
gnomAD v4: 2-210210086-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.210210086A>G , CM000664.2:g.210210086A>G GRCh38
NC_000002.11:g.211074810A>G , CM000664.1:g.211074810A>G GRCh37
NC_000002.10:g.210783055A>G NCBI36
NG_008002.1:g.20406T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000233710.4:c.603+110T>C MANE Select ENSP00000233710.3:n.603+110T>C
ENST00000652584.1:n.831+110T>C
ENST00000233710.3:c.603+110T>C ENSP00000233710.3:n.603+110T>C
ENST00000482502.1:n.550T>C
NM_001608.3:c.603+110T>C NP_001599.1:n.603+110T>C
XM_005246517.3:c.540+110T>C XP_005246574.1:n.540+110T>C
XM_005246517.4:c.540+110T>C XP_005246574.1:n.540+110T>C
XM_017003955.1:c.180+110T>C XP_016859444.1:n.180+110T>C
NM_001608.4:c.603+110T>C MANE Select NP_001599.1:n.603+110T>C
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