Canonical Allele Identifier: CA386601877
Gene: ACADS HGNC NCBI

Linked Data

dbSNP Id: rs1883581146
MyVariant Identifiers: chr12:g.121177157A>C (hg19) chr12:g.120739354A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120739354A>C , CM000674.2:g.120739354A>C GRCh38
NC_000012.11:g.121177157A>C , CM000674.1:g.121177157A>C GRCh37
NC_000012.10:g.119661540A>C NCBI36
NG_007991.1:g.18587A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.1145A>C MANE Select ENSP00000242592.4:p.Tyr382Ser
ENST00000242592.8:c.1145A>C ENSP00000242592.4:p.Tyr382Ser
ENST00000411593.2:c.1133A>C ENSP00000401045.2:p.Tyr378Ser
NM_000017.3:c.1145A>C NP_000008.1:p.Tyr382Ser
NM_001302554.1:c.1133A>C NP_001289483.1:p.Tyr378Ser
NM_000017.4:c.1145A>C MANE Select NP_000008.1:p.Tyr382Ser
NM_001302554.2:c.1133A>C NP_001289483.1:p.Tyr378Ser
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Search 100 bp 3'