Canonical Allele Identifier: CA386601799
Gene: ACADS HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.121177121T>C (hg19) chr12:g.120739318T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120739318T>C , CM000674.2:g.120739318T>C GRCh38
NC_000012.11:g.121177121T>C , CM000674.1:g.121177121T>C GRCh37
NC_000012.10:g.119661504T>C NCBI36
NG_007991.1:g.18551T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000242592.9:c.1109T>C MANE Select ENSP00000242592.4:p.Met370Thr
ENST00000242592.8:c.1109T>C ENSP00000242592.4:p.Met370Thr
ENST00000411593.2:c.1097T>C ENSP00000401045.2:p.Met366Thr
NM_000017.3:c.1109T>C NP_000008.1:p.Met370Thr
NM_001302554.1:c.1097T>C NP_001289483.1:p.Met366Thr
NM_000017.4:c.1109T>C MANE Select NP_000008.1:p.Met370Thr
NM_001302554.2:c.1097T>C NP_001289483.1:p.Met366Thr
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