Canonical Allele Identifier: CA386601812
Gene: ACADS HGNC NCBI

Linked Data

gnomAD v4: 12-120739324-A-C
MyVariant Identifiers: chr12:g.121177127A>C (hg19) chr12:g.120739324A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120739324A>C , CM000674.2:g.120739324A>C GRCh38
NC_000012.11:g.121177127A>C , CM000674.1:g.121177127A>C GRCh37
NC_000012.10:g.119661510A>C NCBI36
NG_007991.1:g.18557A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000242592.9:c.1115A>C MANE Select ENSP00000242592.4:p.Tyr372Ser
ENST00000242592.8:c.1115A>C ENSP00000242592.4:p.Tyr372Ser
ENST00000411593.2:c.1103A>C ENSP00000401045.2:p.Tyr368Ser
NM_000017.3:c.1115A>C NP_000008.1:p.Tyr372Ser
NM_001302554.1:c.1103A>C NP_001289483.1:p.Tyr368Ser
NM_000017.4:c.1115A>C MANE Select NP_000008.1:p.Tyr372Ser
NM_001302554.2:c.1103A>C NP_001289483.1:p.Tyr368Ser
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Search 100 bp 3'