Canonical Allele Identifier: CA244494633
Gene: ACADS HGNC NCBI

Linked Data

dbSNP Id: rs35503787
MyVariant Identifiers: chr12:g.121176616_121176617insT (hg19) chr12:g.120738813_120738814insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120738815dup , CM000674.2:g.120738815dup GRCh38
NC_000012.11:g.121176618dup , CM000674.1:g.121176618dup GRCh37
NC_000012.10:g.119661001dup NCBI36
NG_007991.1:g.18048dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.934-5dup MANE Select ENSP00000242592.4:n.934-5dup
ENST00000242592.8:c.934-5dup ENSP00000242592.4:n.934-5dup
ENST00000411593.2:c.922-5dup ENSP00000401045.2:n.922-5dup
NM_000017.3:c.934-5dup NP_000008.1:n.934-5dup
NM_001302554.1:c.922-5dup NP_001289483.1:n.922-5dup
NM_000017.4:c.934-5dup MANE Select NP_000008.1:n.934-5dup
NM_001302554.2:c.922-5dup NP_001289483.1:n.922-5dup
Search 100 bp 5'
Search 100 bp 3'